Methods and compositions for targeting pd-l1

ABSTRACT

The present disclosure relates to small interfering RNA (siRNA) molecules directed to mRNA transcripts of CD274 to cause downregulation of programmed death-ligand 1 (PD-L1) expression in humans. The siRNA can be constructed of unmodified nucleotides or modified nucleotides that exhibit modified sugars, nucleobases, linkages, or covalently bound targeting moieties. Also disclosed herein are pharmaceutical compositions of siRNAs and uses of or methods of using the siRNAs for the treatment of PD-L1 related diseases including but not limited to liver diseases, cancer, hepatocellular carcinoma, viral diseases, or hepatitis B.

INCORPORATION BY REFERENCE TO PRIORITY APPLICATION

This application claims priority to U.S. Provisional Application Ser. No. 62/983,114, filed Feb. 28, 2020, which is hereby incorporated herein by reference in its entirety.

FIELD

The present application relates to the fields of chemistry, biochemistry, molecular biology and medicine. The present disclosure relates to small interfering RNA (siRNA) molecules directed to mRNA transcripts of CD274 to cause downregulation of programmed death-ligand 1 (PD-L1) expression in humans. The siRNA can be constructed of unmodified nucleotides or modified nucleotides that exhibit modified sugars, nucleobases, linkages, or covalently bound targeting and/or lipophilic moieties. Also disclosed herein are pharmaceutical compositions of siRNAs and uses of or methods of using the siRNAs for the treatment of PD-L1 related diseases including but not limited to liver diseases, cancer, hepatocellular carcinoma, viral diseases, or hepatitis B.

BACKGROUND

The programmed cell death 1 (PD-1) immune checkpoint expressed on the surface of activated CD4⁺ and CD8⁺ T cells controls an inhibitory mechanism to prevent autoimmunity. Engagement of PD-1 by programmed death-ligand 1 (PD-L1) expressed on the multitude of cell types, including macrophages, dendritic cells, mast cells as well as non-hematopoietic cells, induces T cell exhaustion resulting in reduction or loss of effector cytokine production (e.g. IL-2, TNF-α, IFN-γ) and upregulation of other inhibitory receptors and immune checkpoints (e.g. CTLA-4, LAG-3, and BTLA), or T cell apoptosis. High expression of PD-L1 is exhibited by many types of cancers to escape tumor immune surveillance and has been associated with poorer prognosis. PD-1-mediated immunosuppression is also linked to some viral infections, such as hepatitis B. There is an ongoing need for PD-1/PD-L1 therapies and improvements thereof for the treatment of disease.

SUMMARY

Embodiments provided herein related to small interfering RNA (siRNA) molecules that target to CD274, compositions thereof, and uses thereof for the treatment, inhibition, amelioration, prevention or slowing of diseases or conditions associated with PD-L1 dysregulation.

Some embodiments provided herein relate to small interfering RNAs (siRNAs) that targets human CD274 mRNA. In some embodiments, the siRNA comprises a sense strand and an antisense strand. In some embodiments, the antisense strand comprises 18 to 21 nucleotides selected from the group consisting of unmodified nucleotides and modified nucleosides. In some embodiments, each modified nucleoside contains a modified sugar, contains a modified nucleobase or is abasic, or both contains a modified sugar and contains a modified nucleobase or is abasic. In some embodiments, each linkage between the nucleosides is a phosphorothioate, phosphodiester, phosphoramidate, thiophosphoramidate, methylphosphate, methylphosphonate, boranophosphate, or any combination thereof. In some embodiments, the siRNA is at least 85% complementary to a fragment of human CD274 mRNA. In some embodiments, the siRNA comprises zero, one, or two mismatches to the fragment of human CD274 mRNA. In some embodiments, the mismatches occur at any one or more of positions 1 or 9 through m, wherein m is the total number of nucleotides in the antisense strand. In some embodiments, the mismatches do not occur at a seed region of the siRNA. In some embodiments, the seed region is at positions 2-8. In some embodiments, the siRNA has a sequence as set forth in any one of SEQ ID NOs: 2-380. In some embodiments, the siRNA has 18 nucleotides. In some embodiments, the siRNA has 19 nucleotides. In some embodiments, the siRNA has 20 nucleotides. In some embodiments, the siRNA has 21 nucleotides. In some embodiments, the siRNA includes a 2-nucleotide overhang. In some embodiments, the 2-nucleotide overhang is non-complementary to the CD274 mRNA. In some embodiments, the modified sugar is selected from the group consisting of 2′-OMe, 2′-F, 2′-MOE, 2′-araF, 2′-OEt, 2′-O-alkyl, LNA, scpBNA, AmNA, cEt, ENA, and GNA. In some embodiments, the antisense strand comprises a 5′-phosphate group or a 5′-phosphate mimic. In some embodiments, the 5′-phosphate mimic is a 5′-vinylphosponate.

In some embodiments, the siRNA further includes a targeting and/or lipophilic moiety. In some embodiments, the targeting moiety is conjugated to the siRNA at the 5′ end, 3′ end, or both. In some embodiments, the targeting moiety is a fatty acid, GalNAc, folic acid, cholesterol, tocopherol, or palmitate. In some embodiments, the siRNA includes a base selected from the group consisting of adenine, guanine, cytosine, thymine, and uracil.

Some embodiments provided herein relate to pharmaceutical compositions. In some embodiments, the compositions include an effective amount of any siRNA described herein and a pharmaceutically acceptable carrier, diluent, excipient, or combination thereof.

Some embodiments provided herein relate to any siRNA as described herein or any pharmaceutical composition as described herein for use in treating a disorder or disease, such as an infection or a cancer, such as for use in treating hepatitis B or for use in treating hepatocellular carcinoma (HCC). In some embodiments, the siRNA is used in combination with surgery, radiation therapy, chemotherapy, targeted therapy, immunotherapy, hormonal therapy, or antiviral therapy. In some embodiments, the siRNA comprises an siRNA against PD-L1 and an siRNA or an antisense oligonucleotide (ASO) against hepatitis B virus (HBV).

Some embodiments provided herein relate to methods for treating a disease or disorder in a subject. In some embodiments, the methods include administering to the subject an effective amount of any siRNA as described herein or an effective amount of any pharmaceutical composition as described herein. In some embodiments, the disease or disorder is an infection or a cancer, such as hepatitis B or hepatocellular carcinoma. In some embodiments, the methods further include administering surgery, radiation therapy, chemotherapy, targeted therapy, immunotherapy, hormonal therapy, or antiviral therapy.

Additional embodiments are described in greater detail below.

BRIEF DESCRIPTION OF THE DRAWINGS

In addition to the features described above, additional features and variations will be readily apparent from the following descriptions of the drawings and exemplary embodiments. It is to be understood that these drawings depict typical embodiments, and are not intended to be limiting in scope.

FIG. 1 depicts fraction of PD-L1 mRNA remaining in siRNA treated human hepatocellular carcinoma cells (SNU-387 cells) after treatment with exemplary modified siRNA sequences provided herein.

FIG. 2 depicts relative gene expression for PD-L1 RNA in mouse liver 72 hours after treatment with exemplary modified siRNA sequences provided herein.

DETAILED DESCRIPTION

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art. All patents, applications, published applications and other publications referenced herein are expressly incorporated by reference in their entireties unless stated otherwise. In the event that there is a plurality of definitions for a term herein, those in this section prevail unless stated otherwise.

The articles “a” and “an” are used herein to refer to one or to more than one (for example, at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.

The terms “about” or “around” as used herein refer to a quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length that varies by as much as 30, 25, 20, 15, 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1% to a reference quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length.

Throughout this specification, unless the context requires otherwise, the words “comprise,” “comprises,” and “comprising” will be understood to imply the inclusion of a stated step or element or group of steps or elements but not the exclusion of any other step or element or group of steps or elements.

By “consisting of” is meant including, and limited to, whatever follows the phrase “consisting of.” Thus, the phrase “consisting of” indicates that the listed elements are required or mandatory, and that no other elements may be present. By “consisting essentially of” is meant including any elements listed after the phrase and limited to other elements that do not interfere with or contribute to the activity or action specified in the disclosure for the listed elements. Thus, the phrase “consisting essentially of” indicates that the listed elements are required or mandatory, but that other elements are optional and may or may not be present depending upon whether or not they materially affect the activity or action of the listed elements.

The practice of the present disclosure will employ, unless indicated specifically to the contrary, conventional methods of molecular biology and recombinant DNA techniques within the skill of the art.

Hepatocellular carcinoma (HCC) is the most common form of liver cancer. HCC can be caused by a variety of conditions, such as alcohol consumption, cirrhosis, and viral infections that cause hepatitis, such as hepatitis B virus, hepatitis C virus, and hepatitis D virus. The inflammation, fibrosis, and cirrhosis linked with these conditions can induce malignancies in affected liver cells. HCC has relatively poor prognosis, with a five-year survival rate of about 30%, depending on if full surgical resection of the tumor is possible.

For early disease, surgical resection is used. However, most HCC are identified at later stages because of difficulties in diagnosing. Upon late stage diagnosis, the tumors are unresectable, and most patients are given systemic therapies. The current standard of care in front line are multi-kinase inhibitors (including, for example, sorafenib and/or lenvatinib). Most patients are refractory or relapse from these treatments, and undergo second line therapies that have anti-angiogenic agents (including, for example, Regorafinib, Cabozantinib, and/or Ramicirumab) or immune checkpoint inhibitors (including, for example, nibolumab and/or pembrolizumab). However, most patients do not respond to first and second therapies, and the clinical benefit is poor, with overall survival not exceeding one year. In addition, biomarker driven therapies are lacking. Thus, there is a need to develop more tolerable and efficacious therapies for the treatment of HCC and related liver disorders.

HBV is a partially double-stranded circular DNA of about 3.2 kilobase (kb) pairs, and is classified into eight genotypes, A to H. The HBV replication pathway has been studied in great detail. One part of replication includes the formation of the covalently closed circular DNA (cccDNA) form. The presence of the cccDNA gives rise to the risk of viral reemergence throughout the life of the host organism. HBV carriers can transmit the disease for many years. An estimated 300 million people are living with hepatitis B virus infection, and it is estimated that over 750,000 people worldwide die of hepatitis B each year. In addition, immunosuppressed individuals or individuals undergoing chemotherapy are especially at risk for reactivation of an HBV infection. HBV can be acute and/or chronic. Acute HBV infection can be either asymptomatic or present with symptomatic acute hepatitis.

HBV can be transmitted by blood, semen, and/or another body fluid. This can occur through direct blood-to-blood contact, unprotected sex, sharing of needles, and from an infected mother to her baby during the delivery process. The HBV surface antigen (HBsAg) is most frequently used to screen for the presence of this infection. Currently available medications do not cure HBV and/or HDV infection. Rather, the medications suppress replication of the virus.

The hepatitis D virus (HDV) is a DNA virus, also in the Hepadnaviridae family of viruses. HDV can propagate only in the presence of HBV. The routes of transmission of HDV are similar to those for HBV. Transmission of HDV can occur either via simultaneous infection with HBV (coinfection) or in addition to chronic hepatitis B or hepatitis B carrier state (superinfection). Both superinfection and coinfection with HDV results in more severe complications compared to infection with HBV alone. These complications include a greater likelihood of experiencing liver failure in acute infections and a rapid progression to liver cirrhosis, with an increased risk of developing liver cancer in chronic infections. In combination with hepatitis B, hepatitis D has the highest fatality rate of all the hepatitis infections, at 20%. There is currently no cure or vaccine for hepatitis D.

Programmed cell death 1, or programmed death 1 (PD-1) is a 268 amino acid long type I transmembrane protein found as a surface marker on T cells and other immune cells. As an immune checkpoint, PD-1 serves to negatively regulate immune responses to prevent autoimmune disorder. PD-1 protein (NCBI accession number NP_005009.2) is expressed from the cluster of differentiation 279 (CD279) gene (NCBI accession number NG_012110.1) or mRNA transcript (NCBI accession number NM_005018.3). In some preferred embodiments, PD-1 is the human PD-1 protein, and CD279 is the human CD279 transcript or gene on chromosome 2. It should be understood that a person with ordinary skill in the art would view the terms PD-1 and CD279 as often nominally interchangeable when considering the nucleic acid (DNA or RNA) or corresponding translated protein, or the sequences thereof.

Programmed cell death-ligand 1, or programmed death-ligand 1 (PD-L1), also known as B7 homolog 1 (B7-H1) is 272 amino acid long type I transmembrane protein found as a surface marker on many different cell types. PD-L1 is a major ligand of PD-1 and results in inhibition of T cell cytotoxicity and cytokine production. Cancer cells such as HCC cells take advantage of this immune checkpoint by upregulating PD-L1 expression, resulting in dysfunctional anti-tumor immunity by proximal T cells. Viruses also have been observed to modulate the PD-1/PD-L1 pathway to improve infectivity. Hepatitis B virus has been shown to upregulate PD-L1 in infected hepatocytes, and PD-1 in associated T cells. PD-L1 protein (NCBI accession number NP_054862.1) is expressed from the cluster of differentiation 274 (CD274) transcript (NCBI accession number NM_014143.4). In some preferred embodiments, PD-L1 is the human PD-L1 protein, and CD274 is the human CD274 transcript or gene on chromosome 9. It should be understood that a person with ordinary skill in the art would view the terms PD-L1 and CD274 as often nominally interchangeable when considering the nucleic acid (DNA or RNA) or corresponding translated protein, or the sequences thereof.

As used herein, an “oligonucleotide” refers to a single stranded nucleic acid molecule that includes unmodified nucleotides, modified nucleotides or a combination of modified nucleotides and unmodified nucleotides. In the context of siRNA, an oligonucleotide refers to a strand of the siRNA, such as the sense strand (S strand) or the antisense strand (AS strand).

As used herein, an “unmodified nucleotide” is a nucleotide that has a deoxyribose sugar or a ribose sugar and a nucleobase selected from adenine, cytosine, guanine, thymine and uracil. An unmodified nucleotide can also be considered to have a nucleoside selected from cytidine, uridine, 5-methyluridine, guanosine and adenosine, deoxycytidine, deoxyuridine, deoxyguanosine, deoxyadenosine, and thymidine. The structures of deoxyribose, ribose, adenine, cytosine, guanine, thymine, uracil, cytidine, uridine, 5-methyluridine, guanosine, adenosine, deoxycytidine, deoxyuridine, deoxyguanosine, deoxyadenosine, and thymidine are known to those skilled in the art.

As used herein, a “deoxyribose sugar” has the structure

B indicates a nucleobase.

As used herein, a “ribose sugar” has the structure

B indicates a nucleobase.

Relevant positions of the 5-membered sugar ring is provided:

As used herein, “modified nucleoside”, or “modified nucleotide” when involving the 3′ or 5′ linkage, refers to a nucleoside that (a) includes or contains a modified sugar, (b) includes or contains a modified base or is abasic, or (c) both (a) includes or contains a modified deoxyribose and (b) includes or contains a modified base or is abasic. A modified sugar refers to either a modified deoxyribose sugar or modified ribose sugar.

As used herein, the term “modified deoxyribose” refers to a deoxyribose sugar that is substituted at one or more positions with a non-hydrogen substituent. The modifications on the deoxy sugar ring can be at any position of the ring, including at the 2′-carbon. As used herein, the term “modified ribose sugar” refers to a ribose sugar that is substituted at one or more positions with a non-hydrogen substituent. The modifications on the deoxyribose sugar or ribose sugar can be at any position of the ring, including at the 2′-carbon.

Examples of modified sugars include but are not limited to 2′-deoxy-2′-fluoro ribose (2′-F), 2′-deoxy-2′-fluoro-arabinonucloetide (2′-araF), 2′-arabinonucleotide (2′-araOH), 2′-O-methyl ribose (2′-OMe), 2′-O-(2-methoxyethyl) ribose (2′-MOE), locked nucleic acid (LNA), 2′-O-ethyl ribose (2′-OEt), 2′-O-alkyl, (5)-constrained ethyl (cEt), ethylene-bridged nucleic acid (ENA), 4′-C-spirocyclopropylene bridged nucleic acid (scpBNA), amido-bridged nucleic acid (AmNA), unlocked nucleic acid (UNA), and glycol nucleic acid (GNA).

As used herein, “2′-F” refers to a modified deoxyribose sugar that has 2′ fluorine substitution and has the structure

As used herein, “2′-araF” refers to a modified ribose sugar that has a fluorine group attached to 2′ position, and has the structure

As used herein, “2′-araOH” refers to a modified ribose sugar that has a hydroxy group attached to 2′ position, and has the structure

As used herein, “2′-OMe” refers to a modified ribose sugar that has a methyl group attached to the 2′ hydroxyl and has the structure

As used herein, “2′-MOE” refers to a modified ribose sugar that has a 2-methoxyethyl group attached to the 2′ hydroxyl and has the structure

As used herein, a “locked nucleic acid” or “LNA” refers to a modified ribose sugar that includes a linkage that connects the 2′-position to the 4′-position of the 5-membered ring. Examples of locked nucleic acids include

and those described in PCT publications WO 2011/052436, WO 2014/046212, and WO 2015/125783, each of which are hereby expressly incorporated by reference for the purpose of their disclosure of LNAs.

As used herein, “2′-O-Ethyl” refers to a modified ribose sugar that has an ethyl group attached to the 2′ hydroxyl and has the structure

As used herein, “cEt” refers to a modified ribose sugar that includes a methyl that bridges the 2′ hydroxyl and the 4′ carbon, and has the structure

As used herein, “scpBNA” refers to a modified ribose sugar where a cyclopropane bridges the 2′ hydroxyl and 4′ carbon and has the structure

As used herein, “AmNA” refers to a modified ribose sugar where the 2′ and 4′ carbon are bridged with an amide bond and has the structure

As used herein, an “unlocked nucleic acid” or “UNA” refers to a modified nucleotide wherein the bond between the 2′-position and the 3′-position of the 5-membered sugar ring is not present (acyclic ribose), and has the structure

In each of the structures, the “Base”, referring to a nucleobase, can be an unmodified base, a modified base or absent, such that the nucleotide is abasic. When not indicated, the nucleotide may be an unmodified nucleotide, modified nucleotide, or abasic.

A “modified base” refers to any base other than adenine, cytosine, guanine, thymine and uracil. For example, a modified base can be a substituted adenine, a substituted cytosine, a substituted 5-methylcytosine, a substituted guanine, a substituted thymine, or a substituted uracil. Alternatively, a modified base can make up a modified nucleoside such as a substituted cytidine, a substituted 5-methyl-cytidine, a substituted uridine, a substituted 5-methyluridine, a substituted guanosine, a substituted adenosine, a substituted deoxycytidine, a substituted 5-methyl-deoxycytidine, a substituted deoxyuridine, a substituted deoxyguanosine, a substituted deoxyadenosine, or a substituted thymidine.

When a specific linkage between the nucleotides are not specified, the linkage may be a phosphodiester or a non-phosphodiester linkage and may be a 3′-5′ linkage and 2′-5′ linkage, such as a phosphorothioate, a methylphosphonate, a phosphoramidate, a thiophosphoramidate, a phosphonoacetate, an amide linkage, or a boranophosphate linkage. The phosphodiester can have the structure

As used herein, a phosphorothioate is used as understood by those skilled in the art and refers to a phosphate wherein one oxygen is replaced with a sulfur. The phosphorothioate can have the structure

As used herein, a methylphosphonate is used as understood by those skilled in the art and refers to a phosphate wherein one oxygen is replaced with a methyl. The methylphosphonate can have the structure

As used herein, a phosphoramidate is used as understood by those skilled in the art and refers to a phosphate wherein one oxygen is replaced with an amide. The phosphoramidate can have the structure

As used herein, a thiophosphoramidate is used as understood by those skilled in the art and refers to a phosphate wherein one oxygen is replaced with a sulfur and one oxygen is replaced with an amide. The thiophosphoramidate can have the structure

As used herein, a phosphonoacetate is used as understood by those skilled in the art and refers to a phosphate wherein one oxygen is replaced with a —CH₂—C(═O)O⁻ or

-   -   CH₂—C(═O)OH. The phosphonoacetate can have the structure

As used herein, an amide linkage is used as understood by those skilled in the art and refers to an amide. The amide linkage can have the structure

As used herein, a boranophosphate is used as understood by those skilled in the art and refers to a phosphate, wherein one oxygen is replace with a boron group. The boranophosphate can have the structure

In some embodiments, the nucleosides are linked with all phosphodiester linkages. In some embodiments, the nucleosides are linked with all phosphorothioate linkages. In some embodiments, the nucleosides are linked with all methylphosphonate linkages. In some embodiments, the nucleosides are linked with all phosphoramidate linkages. In some embodiments, the nucleosides are linked with all thiophosphoramidate linkages. In some embodiments, the nucleosides are linked with all phosphonoacetate linkages. In some embodiments, the nucleosides are linked with all amide linkages. In some embodiments, the nucleosides are linked with all boranophosphate linkages. In some embodiments, the nucleosides are linked with a combination of phosphodiester and phosphorothioate linkages. In some embodiments, the nucleosides are linked with a combination of phosphodiester, phosphorothioate, methylphosphonate, phosphoramidate, thiophosphoramidate, phosphonoacetate, amide, and boranophosphate linkages, including combinations where at least one type of linkage is not present.

Those skilled in the art understand that when the linkage is a non-phosphodiester linkage, the phosphorus can be a chiral center. For example, in a phosphorothioate, the phosphorus can be a (R)-stereocenter or a (S)-stereocenter. In some embodiments, each phosphorus of a non-phosphodiester linkage can be a (R)-stereocenter. In other embodiments, each phosphorus of a non-phosphodiester linkage can be a (S)-stereocenter. For example, in an oligonucleotide that has a phosphorothioate between each nucleotide, each phosphorothioate can be in the (S)-configuration. In still other embodiments, the oligonucleotide can include at least one non-phosphodiester linkage, wherein the phosphorus can be a (S)-stereocenter, and at least one non-phosphodiester linkage, wherein the phosphorus can be a (R)-stereocenter. In some embodiments, a particular linkage within an oligonucleotide may be present in a racemic mixture. In some embodiments, a particular linkage within an oligonucleotide may be present in an unequal mixture of (R) and (S) stereoisomers. For example, a particular linkage may be present where the ratio between (R) and (S) stereoisomers is 0%:100%, 10%:90%, 20%:80%, 30%:70%, 40%:60%, 50%:50%, 60%:40%, 70%:30%, 80%:20%, 90%:10%, 100%:0%, or any ratio in the range defined between any two aforementioned ratios. In some embodiments, a particular linkage within an oligonucleotide is enantiomerically pure, (R) enantiomerically pure, or (S) enantiomerically pure.

It is understood that, in any compound described herein having one or more chiral centers, if an absolute stereochemistry is not expressly indicated, then each center may independently be of (R)-configuration or (S)-configuration or a mixture thereof. Thus, the compounds provided herein may be enantiomerically pure, enantiomerically enriched, racemic mixture, diastereomerically pure, diastereomerically enriched, or a stereoisomeric mixture. Likewise, it is understood that, in any compound described, all tautomeric forms are also intended to be included.

As used herein, the term “small interfering RNA” or “siRNA” has its ordinary meaning as understood in light of the specification, and refers to a class of double-stranded RNA molecules, which interferes with the expression of specific genes having a nucleotide sequence complementary to the siRNA. siRNAs typically have a well-defined structure: a short double-stranded RNA (dsRNA) with phosphorylated 5′ ends and hydroxylated 3′ ends with two overhanging nucleotides. The Dicer enzyme catalyzes production of siRNAs from long dsRNAs and small hairpin RNAs (shRNAs). Double stranded siRNA associates with the RNA-inducing silencing complex (RISC), one strand (the passenger, or sense strand) is lost, and the remaining strand (the guide strand, or antisense strand) cooperates with RIS to bind complementary target RNA. In some embodiments, the siRNA disclosed herein may include about 15 to about 35 base pairs, such as 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, or 35 base pairs in length. In some embodiments, the siRNA antisense strand is complementary to a fragment or portion of target mRNA, such as CD274 mRNA, for initiating transcriptional silencing. In some embodiments, the siRNA provided herein includes a modification. In some embodiments, any of the modifications described herein are applied to the sense strand. In some embodiments, any of the modifications described herein are applied to the antisense strand. In some embodiments, the modification confers one or more beneficial characteristics to the siRNA, such as limiting degradation of the siRNA, improving half-life of the siRNA, increasing potency, activity, stability, safety, efficacy, solubility, permeability, selectivity, bioavailability, or melting temperature.

In some embodiments, the antisense strand of the siRNA includes a 5′-phosphate. In some embodiments, the antisense strand of the siRNA includes a 5′-phosphate mimic. The phosphate or phosphate mimic includes OC- and/or β-configuration with respect to the sugar ring or combinations thereof. The phosphate or phosphate mimics is a natural phosphate, phosphorothioate, phosphorodithioate, boranophosphate, boranothiophosphate, phosphonate, halogen substituted phosphonates, phosphoramidates, phosphodiester, phosphotriester, thiophosphodiester, thiophosphotriester, diphosphates, and/or triphosphates. Suitable phosphate mimics include 5′-phosphonates, such as 5′-methylenephosphonate (5′-MP) and 5′-(E)-vinylphosphonate (5′-VP), and 4′-phosphate analogs that are bound to the 4′-carbon of the sugar moiety (e.g., a ribose or deoxyribose or analog thereof) of the 5′-terminal nucleotide of an oligonucleotide, such as 4′-oxymethylphosphonate, 4′-thiomethylphosphonate, or 4′-aminomethylphosphonate. In some embodiments, the 5′-phosphate mimic is a 5′-vinylphosphonate.

The siRNA can be modified with at least one moiety, such as a targeting moiety. In some embodiments, the targeting moiety is a lipophilic moiety. In some embodiments, the targeting moiety is a long chain fatty acid having a general structure of CH₃(CH₂)_(n)(CH)_(m)COOH, wherein n is a whole number ranging from 1 to 30, and wherein m is a whole number ranging from 1 to 30. Examples of a targeting moiety include, but are not limited to N-acetylgalactosamine (GalNAc, including, for example, a triantennary-GalNAc, including, for example, GalNAc3, GalNAc4, GalNAc5, GalNAc6 and/or GalNAc7), folic acid, cholesterol, tocopherol, vitamin E, or palmitate. Additional examples of long chain fatty acids include, but are not limited to, docohexanoic acid, docosanoic acid, linoleic acid (omega-6), linolenic acid (omega-3), oleic acid, octanoic acid, decanoyl acid, dodecanoyl acid, stearic acid, eicosanoic acid, and arachidonic acid. In some embodiments, the targeting moiety results in preferential targeting of the siRNA to a certain organ or tissue, such as the liver, heart, lung, brain, bone, muscle, kidney, stomach, small intestine, large intestine, or pancreas. In some embodiments, a targeting moiety is conjugated to the 5′ end of the siRNA. In some embodiments, a targeting moiety is conjugated to the 5′ phosphate of the siRNA. In some embodiments, a targeting moiety is conjugated to the 3′ end of the siRNA. In some embodiments, a targeting moiety is conjugated to the 3′ sugar hydroxyl of the siRNA. In some embodiments, a targeting moiety is conjugated to the 5′ end and another targeting moiety is conjugated to the 3′ end of the siRNA. In some embodiments, a second targeting moiety can be conjugated to a first targeting moiety. In some embodiments, a targeting moiety is attached with a linker. In some embodiments, the linker is a nucleotide, such as adenine, guanine, cytosine, thymine, or uracil nucleotides, or non-nucleoside linkers, including triethylene glycol (TEG), hexaethylene glycol (HEG), or alkyl amino linker.

GalNAc as used herein has the following structure

wherein R is OH or SH, and wherein n is any integer. In some embodiments, the deoxycytosine nucleotide shown in this structure linking the siRNA to the GalNAc moiety is optional, and can be omitted. In some embodiments, n ranges from 0 to 10, such as 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. For example, for GalNAc4, n=1; and for GalNAc6, n=2. However, it is to be understood that n may equal any integer and may be selected based on the desired characteristic of the targeting moiety.

As used herein, the term “Xmer” refers to an oligonucleotide or nucleic acid polymer that is “X” nucleotides long. For example, a 14mer is an oligonucleotide or nucleic acid polymer that is 14 nucleotides long, and a 20mer is an oligonucleotide or nucleic acid polymer that is 20 nucleotides long. In some embodiments, the “X” refers to the total number of nucleotides. In other embodiments, the “X” refers to the number of nucleotides involved in binding to the target, while the oligonucleotide or nucleic acid polymer may have additional nucleotides or components that are not involved in binding to the target.

In some embodiments, at least one siRNA is used to treat liver disease. In some embodiments, the liver disease includes but is not limited to liver cancer, hepatocellular carcinoma (HCC), cholangiocarcinoma, hepatitis, hepatitis A, hepatitis B, hepatitis C, hepatitis D, or any combination thereof. In some embodiments, the at least one siRNA is used to silence expression of a gene involved in a liver disease. In some embodiments, the gene is CD274. In some embodiments, the at least one siRNA results in at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% reduction in the disease or symptoms thereof, or in an amount within a range defined by any two of the aforementioned values.

The term “isolated” as used herein refers to material that is substantially or essentially free from components that normally accompany it in its native state. For example, an “isolated cell,” as used herein, includes a cell that has been purified from the milieu or organisms in its naturally occurring state, a cell that has been removed from a subject or from a culture, for example, it is not significantly associated with in vivo or in vitro substances.

As used herein, the abbreviations for any protective groups and other compounds are used, unless indicated otherwise, in accord with their common usage.

It is to be understood that where compounds disclosed herein have unfilled valencies, then the valencies are to be filled with hydrogen or isotopes thereof, e.g., hydrogen-1 (protium) and hydrogen-2 (deuterium).

It is understood that the compounds described herein can be labeled isotopically. Substitution with isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability, such as, for example, increased in vivo half-life or reduced dosage requirements. Each chemical element as represented in a compound structure may include any isotope of said element. For example, in a compound structure a hydrogen atom may be explicitly disclosed or understood to be present in the compound. At any position of the compound that a hydrogen atom may be present, the hydrogen atom can be any isotope of hydrogen, including but not limited to hydrogen-1 (protium) and hydrogen-2 (deuterium). Thus, reference herein to a compound encompasses all potential isotopic forms unless the context clearly dictates otherwise.

Where a range of values is provided, it is understood that the upper and lower limit, and each intervening value between the upper and lower limit of the range is encompassed within the embodiments.

siRNA Synthesis

Each of 2′-OMe, 2′-MOE, and LNA phosphoramidite monomers were procured from commercially-available sources. All the monomers were dried in vacuum desiccator with desiccants (P205, RT 24 h). Universal solid supports (CPG) attached were obtained from ChemGenes. The chemicals and solvents for synthesis workflow were purchased from VWR/Sigma commercially-available sources and used without any purification or treatment. Solvent (Acetonitrile) and solutions (amidite and activator) were stored over molecular sieves during synthesis.

The control and target oligonucleotide sequences were synthesized on an Expedite 8909 synthesizer using the standard cycle written by the manufacturer with modifications as needed to wait steps and coupling steps. The solid support was controlled pore glass and the monomers contained standard protecting groups. Each chimeric oligonucleotide was individually synthesized using commercially available 5′-O-(4,4′-dimethoxytrityl)-3′-O-(2-cyanoethyl-N, N-diisopropyl) DNA, 2′-OMe, 2′-MOE and or LNA phosphoramidite monomers of 6-N-benzoyladenosine (A^(Bz)), 4-N-acetylcytidine (C^(Ac)), 2-N-isobutyrylguanosine (G^(iBu)), and Uridine (U) or Thymidine (T), according to standard solid phase phosphoramidite synthesis protocols. The 2′-O-Me-2,6, diaminopurine phosphoramidite was purchased from Glen Research. The phosphoramidites were prepared as 0.1 M solutions in anhydrous acetonitrile. 5-Ethylthiotetrazole was used as activator, 3% Dichloroacetic acid in dichloromethane was used to detritylate, acetic anhydride in THF and 16% N-methylimidazole in THF were used to cap, and DDTT ((dimethylamino-methylidene) amino)-3H-1,2,4-dithiazaoline-3-thione was used as the sulfur-transfer agent for the synthesis of oligoribonucleotide phosphorothioates. An extended coupling of 0.1M solution of phosphoramidite in CH₃CN in the presence of 5-(ethylthio)-1H-tetrazole activator to a solid bound oligonucleotide followed by extended capping, oxidation and deprotection to afford the modified oligonucleotides. The stepwise coupling efficiency of all modified phosphoramidites was more than 98.5%.

Deprotection and cleavage from the solid support was achieved with mixture of ammonia methylamine (1:1, AMA) for 15 min at 65° C., when the universal linker was used, the deprotection was left for 90 min at 65° C. or solid supports were heated with aqueous ammonia (28%) solution at 55° C. for 8 h to deprotect the base labile protecting groups. After filtering to remove the solid support, the deprotection solution was removed under vacuum in a GeneVac centrifugal evaporator. Tables 1-3 depicts exemplary structures of 2′-OMe, 2′-MOE, and LNA phosphoramidite monomers

TABLE 1 2′-OMe Phosphoramidite Monomers 2′-OMe-A Phosphoramidite

2′-OMe-C Phosphoramidite

2′-OMe-G Phosphoramidite

2′-OMe-U Phosphoramidite

TABLE 2 2′-MOE Phosphoramidite Monomers 2′-MOE-A Phosphoramidite

2′-MOE-(5m)C Phosphoramidite

2′-MOE-G Phosphoramidite

2′-MOE-T Phosphoramidite

TABLE 3 2′-LNA Phosphoramidite Monomers LNA-A Phosphoramidite

LNA-(5m)C Phosphoramidite

LNA-G Phosphoramidite

LNA-T Phosphoramidite

The AmNA and Scp-BNA phosphoramidite monomers of 6-N-benzoyladenosine (A^(Bz)), 4-N-acetylcytidine (C^(Ac)), 2-N-isobutyrylguanosine (G^(iBu)), and Thymidine (T) received from LUXNA Technologies. All the monomers were dried in a vacuum desiccator with desiccants (P205, at room temperature for 24 hours). For the AmNA-PS-DNA-PS and scp-BNA-PS-DNA-PS modifications, the synthesis was carried out on a 1 scale in a 3′ to 5′ direction with the phosphoramidite monomers diluted to a concentration of 0.12 M in anhydrous CH₃CN in the presence of 0.3 M 5-(benzylthio)-1H-tetrazole activator (coupling time 16-20 min) to a solid bound oligonucleotide followed by modified capping, oxidation and deprotection to afford the modified oligonucleotides. The stepwise coupling efficiency of all modified phosphoramidites was more than 97%. The DDTT (dimethylamino-methylidene) amino)-3H-1,2,4-dithiazaoline-3-thione was used as the sulfur-transfer agent for the synthesis of the oligoribonucleotide phosphorothioates. Oligonucleotide-bearing solid supports were washed with 20% DEA solution in acetonitrile for 15 min then the column was washed thoroughly with AcCN. The support was heated at 65° C. with Diisopropylamine:water:Methanol (1:1:2) for 5 h in heat block to cleave from the support and deprotect the base labile protecting groups. Tables 4 and 5 depicts exemplary structures of the AmNA and Scp-BNA phosphoramidite monomers.

TABLE 4 am-NCH₃ Phosphoramidite Monomers am-NCH₃-A phosphoramidite

am-NCH₃-(5m)C phosphoramidite

am-NCH₃-G Phosphoramidite

am-NCH₃-T Phosphoramidite

TABLE 5 Scp-BNA Phosphoramidite Monomers Scp-BNA-A phosphoramidite

Scp-BNA-(5m)C phosphoramidite

Scp-BNA-G Phosphoramidite

Scp-BNA-T Phosphoramidite

The cholesterol, tocopherol phosphoramidite, and solid supports were received from ChemGenes. The cholesterol and Tocopherol conjugated oligonucleotides were obtained by initiating solid phase synthesis on cholesterol and Tocopherol supports attached on TEG linker for 3′-conjugation while final coupling of the phosphoramidite provided the 5′-conjugated oligonucleotides.

Quantitation of Crude Oligomer or Raw Analysis

Samples were dissolved in deionized water (1.0 mL) and quantified as follows: Blanking was first performed with water alone (1.0 mL), then 20 μL of sample and 980 μL of water were mixed well in a microfuge tube, transferred to cuvette and absorbance reading obtained at 260 nm. The crude material was dried and stored at −20° C.

Crude HPLC/LC-MS Analysis

The 0.1 OD of the crude samples were used for crude MS analysis. After confirming the crude LC-MS data, the purification step was performed.

HPLC Purification

The Phosphodiester (PO), Phosphorothioate (PS) and chimeric modified oligonucleotides were purified by anion-exchange HPLC. The buffers were 20 mM sodium phosphate in 10% CH₃CN, pH 8.5 (buffer A) and 20 mM sodium phosphate in 10% CH₃CN, 1.8 M NaBr, pH 8.5 (buffer B). Fractions containing full-length oligonucleotides were pooled, desalted and lyophilized.

The conjugated oligonucleotides were purified by an in-house packed RPC-Source15 reverse-phase column. The buffers were 20 mM sodium acetate in 10% CH₃CN, (buffer A) and CH₃CN (buffer B). Fractions containing full-length oligonucleotides were pooled, desalted and lyophilized.

Desalting of Purified Oligomer

The purified dry oligomer was then desalted using Sephadex G-25 M (Amersham Biosciences). The cartridge was conditioned with 10 mL of deionized water thrice. The purified oligonucleotide dissolved thoroughly in 2.5 mL deionized water was applied to the cartridge with very slow drop wise elution. The salt free oligomer was eluted with 3.5 mL deionized water directly into a screw cap vial.

Final HPLC and Electrospray LC/MS Analysis

Approximately 0.10 OD of oligomer is dissolved in water and then pipetted in special vials for IEX-HPLC and LC/MS analysis. Analytical HPLC and ES LC-MS established the integrity of the chimeric oligonucleotides.

The cholesterol and tocopherol conjugated sequences were analyzed by high-performance liquid chromatography (HPLC) on a Luna C8 reverse-phase column. The buffers were 20 mM NaOAc in 10% CH₃CN (buffer A) and 20 mM NaOAc in 70% CH₃CN (buffer B). Analytical HPLC and ES LC-MS established the integrity of the conjugated oligonucleotides

Post Synthesis Conjugation:

5′-Folate conjugated siRNAs: To a solution of 5′-hexylamino siRNA in 0.1 M sodium tetraborate buffer, pH 8.5 (2 mM) a solution of Folate-NHS ester (3 mole equivalent) dissolved in DMSO (40 mM) was added, and the reaction mixture was stirred at room temperature for 3 h. The Reaction mixture concentrated under reduced pressure. The residue was dissolved in water and purified by HPLC on a strong anion exchange column (GE Healthcare Bioscience, Source 30Q, 30 μm, 2.54×8 cm, A=100 mM ammonium acetate in 30% aqueous CH₃CN, B=1.8 M NaBr in A, 0-60% of B in 60 min, flow 10 mL/min). The residue was desalted by in house packed Sephadex G-25 column to yield the 5′-Folate conjugated siRNAs in an isolated yield of 62-80%. The folate conjugated siRNAs were characterized by IEX-HPLC and Thermo Fischer ESI-LC-MS system. Table 6 depicts exemplary nucleic acids and structures.

TABLE 6 Abbreviations for nucleic acid structures Abbreviation Name Structure A Adenine

G Guanine

C Cytosine

U Uracil

T Thymine

(5m)C 5-methyl-cytosine

DAP 2,6-diaminopurine

d Deoxy

ps Phosphorothioate

ln LNA

am AmNA

scp Scp-BNA

m 2′-OMe

moe 2′-MOE

cet cEt

gn GNA

Any of the structures shown in Table 6 can be combined with any base, thereby generating various combinations of structures. For example, using the abbreviations and structures from Table 6, one skilled in the art understands that the abbreviation “AmG” represents

Furthermore, additional structures not depicted in the tables, but described elsewhere throughout the application may be used and combined with any base described in the tables or elsewhere throughout the application.

Pharmaceutical Compositions

Some embodiments described herein relate to pharmaceutical compositions that comprise, consist essentially of, or consist of an effective amount of an siRNA described herein and a pharmaceutically acceptable carrier, excipient, or combination thereof. A pharmaceutical composition described herein is suitable for human and/or veterinary applications.

The terms “function” and “functional” as used herein refer to a biological, enzymatic, or therapeutic function.

The terms “effective amount” or “effective dose” is used to indicate an amount of an active compound, or pharmaceutical agent, that elicits the biological or medicinal response indicated. For example, an effective amount of compound can be the amount needed to alleviate or ameliorate symptoms of disease or prolong the survival of the subject being treated This response may occur in a tissue, system, animal or human and includes alleviation of the signs or symptoms of the disease being treated. Determination of an effective amount is well within the capability of those skilled in the art, in view of the disclosure provided herein. The effective amount of the compounds disclosed herein required as a dose will depend on the route of administration, the type of animal, including human, being treated, and the physical characteristics of the specific animal under consideration. The dose can be tailored to achieve a desired effect, but will depend on such factors as weight, diet, concurrent medication and other factors which those skilled in the medical arts will recognize.

The term “pharmaceutically acceptable salts” includes relatively non-toxic, inorganic and organic acid, or base addition salts of compositions, including without limitation, analgesic agents, therapeutic agents, other materials, and the like. Examples of pharmaceutically acceptable salts include those derived from mineral acids, such as hydrochloric acid and sulfuric acid, and those derived from organic acids, such as ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, and the like. Examples of suitable inorganic bases for the formation of salts include the hydroxides, carbonates, and bicarbonates of ammonia, sodium, lithium, potassium, calcium, magnesium, aluminum, zinc, and the like. Salts may also be formed with suitable organic bases, including those that are non-toxic and strong enough to form such salts. For example, the class of such organic bases may include but are not limited to mono-, di-, and trialkylamines, including methylamine, dimethylamine, and triethylamine; mono-, di-, or trihydroxyalkylamines including mono-, di-, and triethanolamine; amino acids, including glycine, arginine and lysine; guanidine; N-methylglucosamine; N-methylglucamine; L-glutamine; N-methylpiperazine; morpholine; ethylenediamine; N-benzylphenethylamine; trihydroxymethyl aminoethane.

“Formulation”, “pharmaceutical composition”, and “composition” as used interchangeably herein are equivalent terms referring to a composition of matter for administration to a subject.

The term “pharmaceutically acceptable” means compatible with the treatment of a subject, and in particular, a human.

The terms “agent” refers to an active agent that has biological activity and may be used in a therapy. Also, an “agent” can be synonymous with “at least one agent,” “compound,” or “at least one compound,” and can refer to any form of the agent, such as a derivative, analog, salt or a prodrug thereof. The agent can be present in various forms, components of molecular complexes, and pharmaceutically acceptable salts (e.g., hydrochlorides, hydrobromides, sulfates, phosphates, nitrates, borates, acetates, maleates, tartrates, and salicylates). The term “agent” can also refer to any pharmaceutical molecules or compounds, therapeutic molecules or compounds, matrix forming molecules or compounds, polymers, synthetic molecules and compounds, natural molecules and compounds, and any combination thereof.

The term “subject” as used herein has its ordinary meaning as understood in light of the specification and refers to an animal that is the object of treatment, inhibition, or amelioration, observation or experiment. “Animal” has its ordinary meaning as understood in light of the specification and includes cold- and warm-blooded vertebrates and/or invertebrates such as fish, shellfish, or reptiles and, in particular, mammals. “Mammal” has its ordinary meaning as understood in light of the specification, and includes but is not limited to mice, rats, rabbits, guinea pigs, dogs, cats, sheep, goats, cows, horses, primates, such as humans, monkeys, chimpanzees, or apes. In some embodiments, the subject is human.

Proper formulation is dependent upon the route of administration chosen. Techniques for formulation and administration of the compounds described herein are known to those skilled in the art. Multiple techniques of administering a compound exist in the art including, but not limited to, enteral, oral, rectal, topical, sublingual, buccal, intraaural, epidural, epicutaneous, aerosol, parenteral delivery, including intramuscular, subcutaneous, intra-arterial, intravenous, intraportal, intra-articular, intradermal, peritoneal, intramedullary injections, intrathecal, direct intraventricular, intraperitoneal, intranasal or intraocular injections. Pharmaceutical compositions will generally be tailored to the specific intended route of administration. Pharmaceutical compositions can also be administered to isolated cells from a patient or individual, such as T cells, Natural Killer cells, B cells, macrophages, lymphocytes, stem cells, bone marrow cells, or hematopoietic stem cells.

The pharmaceutical compound can also be administered in a local rather than systemic manner, for example, via injection of the compound directly into an organ, tissue, cancer, tumor or infected area, often in a depot or sustained release formulation. Furthermore, one may administer the compound in a targeted drug delivery system, for example, in a liposome coated with a tissue specific antibody. The liposomes may be targeted to and taken up selectively by the organ, tissue, cancer, tumor, or infected area.

The pharmaceutical compositions disclosed herein may be manufactured in a manner that is itself known, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or tableting processes. As described herein, compounds used in a pharmaceutical composition may be provided as salts with pharmaceutically compatible counterions.

As used herein, a “carrier” refers to a compound, particle, solid, semi-solid, liquid, or diluent that facilitates the passage, delivery and/or incorporation of a compound to cells, tissues and/or bodily organs. For example, without limitation, a lipid nanoparticle (LNP) is a type of carrier that can encapsulate an oligonucleotide to thereby protect the oligonucleotide from degradation during passage through the bloodstream and/or to facilitate delivery to a desired organ, such as to the liver.

As used herein, a “diluent” refers to an ingredient in a pharmaceutical composition that lacks pharmacological activity but may be pharmaceutically necessary or desirable. For example, a diluent may be used to increase the bulk of a potent drug whose mass is too small for manufacture and/or administration. It may also be a liquid for the dissolution of a drug to be administered by injection, ingestion or inhalation. A common form of diluent in the art is a buffered aqueous solution such as, without limitation, phosphate buffered saline that mimics the composition of human blood.

The term “excipient” has its ordinary meaning as understood in light of the specification, and refers to inert substances, compounds, or materials added to a pharmaceutical composition to provide, without limitation, bulk, consistency, stability, binding ability, lubrication, disintegrating ability etc., to the composition. Excipients with desirable properties include but are not limited to preservatives, adjuvants, stabilizers, solvents, buffers, diluents, solubilizing agents, detergents, surfactants, chelating agents, antioxidants, alcohols, ketones, aldehydes, ethylenediaminetetraacetic acid (EDTA), citric acid, salts, sodium chloride, sodium bicarbonate, sodium phosphate, sodium borate, sodium citrate, potassium chloride, potassium phosphate, magnesium sulfate sugars, dextrose, fructose, mannose, lactose, galactose, sucrose, sorbitol, cellulose, serum, amino acids, polysorbate 20, polysorbate 80, sodium deoxycholate, sodium taurodeoxycholate, magnesium stearate, octylphenol ethoxylate, benzethonium chloride, thimerosal, gelatin, esters, ethers, 2-phenoxyethanol, urea, or vitamins, or any combination thereof. The amount of the excipient may be found in a pharmaceutical composition at a percentage of 0%, 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 100% w/w or any percentage by weight in a range defined by any two of the aforementioned numbers.

The term “adjuvant” as used herein refers to a substance, compound, or material that stimulates the immune response and increase the efficacy of protective immunity and is administered in conjunction with an immunogenic antigen, epitope, or composition. Adjuvants serve to improve immune responses by enabling a continual release of antigen, up-regulation of cytokines and chemokines, cellular recruitment at the site of administration, increased antigen uptake and presentation in antigen presenting cells, or activation of antigen presenting cells and inflammasomes. Commonly used adjuvants include but are not limited to alum, aluminum salts, aluminum sulfate, aluminum hydroxide, aluminum phosphate, calcium phosphate hydroxide, potassium aluminum sulfate, oils, mineral oil, paraffin oil, oil-in-water emulsions, detergents, MF59®, squalene, AS03, α-tocopherol, polysorbate 80, ASO4, monophosphoryl lipid A, virosomes, nucleic acids, polyinosinic:polycytidylic acid, saponins, QS-21, proteins, flagellin, cytokines, chemokines, IL-1, IL-2, IL-12, IL-15, IL-21, imidazoquinolines, CpG oligonucleotides, lipids, phospholipids, dioleoyl phosphatidylcholine (DOPC), trehalose dimycolate, peptidoglycans, bacterial extracts, lipopolysaccharides, or Freund's Adjuvant, or any combination thereof.

The term “purity” of any given substance, compound, or material as used herein refers to the actual abundance of the substance, compound, or material relative to the expected abundance. For example, the substance, compound, or material may be at least 80, 85, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100% pure, including all decimals in between. Purity may be affected by unwanted impurities, including but not limited to side products, isomers, enantiomers, degradation products, solvent, carrier, vehicle, or contaminants, or any combination thereof. Purity can be measured technologies including but not limited to chromatography, liquid chromatography, gas chromatography, spectroscopy, UV-visible spectrometry, infrared spectrometry, mass spectrometry, nuclear magnetic resonance, gravimetry, or titration, or any combination thereof.

Methods of Use

Some embodiments disclosed herein related to selecting a subject or patient in need. In some embodiments, a patient is selected who is in need of treatment, inhibition, amelioration, prevention or slowing of diseases or conditions associated with PD-L1 dysregulation. In some embodiments, such diseases or conditions associated with PD-L1 dysregulation may include, for example, cancer, HCC, viral infections, or HBV. In some embodiments, a patient is selected who has previously been treated for the disease or disorder described herein. In some embodiments, a patient is selected who has previously been treated for being at risk for the disease or disorder described herein. In some embodiments, a patient is selected who has developed a recurrence of the disease or disorder described herein. In some embodiments, a patient is selected who has developed resistance to therapies for the disease or disorder described herein. In some embodiments, a patient is selected who may have any combination of the aforementioned selection criteria.

siRNA molecules and pharmaceutical compositions comprising siRNA molecules disclosed herein can be evaluated for efficacy and toxicity using known methods. A non-limiting list of potential advantages of an siRNA described herein include improved stability, increased safety profile, increased efficacy, increased binding to the target, increased specificity for the target (for example, a cancer cell or virally infected cell).

The terms “treating,” “treatment,” “therapeutic,” or “therapy” as used herein has its ordinary meaning as understood in light of the specification, and do not necessarily mean total cure or abolition of the disease or condition. The term “treating” or “treatment” as used herein (and as well understood in the art) also means an approach for obtaining beneficial or desired results in a subject's condition, including clinical results. Beneficial or desired clinical results can include, but are not limited to, alleviation or amelioration of one or more symptoms or conditions, diminishment of the extent of a disease, stabilizing (i.e., not worsening) the state of disease, prevention of a disease's transmission or spread, delaying or slowing of disease progression, amelioration or palliation of the disease state, diminishment of the reoccurrence of disease, and remission, whether partial or total and whether detectable or undetectable. “Treating” and “treatment” as used herein also include prophylactic treatment. Treatment methods comprise administering to a subject a therapeutically effective amount of an active agent. The administering step may consist of a single administration or may comprise a series of administrations. The compositions are administered to the subject in an amount and for a duration sufficient to treat the patient. The length of the treatment period depends on a variety of factors, such as the severity of the condition, the age and genetic profile of the patient, the concentration of active agent, the activity of the compositions used in the treatment, or a combination thereof. It will also be appreciated that the effective dosage of an agent used for the treatment or prophylaxis may increase or decrease over the course of a particular treatment or prophylaxis regime. Changes in dosage may result and become apparent by standard diagnostic assays known in the art. In some instances, chronic administration may be required.

Some embodiments described herein relate to a method of treating, inhibiting, ameliorating, preventing, or slowing the disease or disorder described herein. In some embodiments, the methods include administering to a subject identified as suffering from the disease or disorder described herein an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA as described herein. Other embodiments described herein relate to using an siRNA as described herein in the manufacture of a medicament for treating, inhibiting ameliorating, preventing, or slowing the disease or disorder described herein. Still other embodiments described herein relate to the use of an siRNA as described herein or a pharmaceutical composition that includes an effective amount of an siRNA as described herein for treating, inhibiting ameliorating, preventing, or slowing the disease or disorder described herein.

Some embodiments described herein relate to a method for inhibiting replication of a cancer cell or a virus that can include contacting the cell or virus or administering to a subject identified as suffering from a cancer or a viral infection with an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA described herein. Other embodiments described herein relate to the use of an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA described herein in the manufacture of a medicament for inhibiting replication of a cancer cell or virus. Still other embodiments described herein relate to an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA described herein for inhibiting replication of a cancer cell or virus. In some embodiments, the cancer cell is an HCC cell. In some embodiments, the virus is hepatitis B.

Some embodiments described herein relate to a method for inhibiting cell proliferation, such as inhibiting cell proliferation of a cancer cell or cell infected with a virus, that can include administering to a subject identified as suffering from a disease wherein inhibiting cell proliferation is desirable with an effective amount of an siRNA described herein, or a pharmaceutical composition that includes effective amount of an siRNA described herein. Other embodiments described herein relate to the use of an effective amount of an oligonucleotide described herein, or a pharmaceutical composition that includes an effective amount of an siRNA described herein in the manufacture of a medicament for inhibiting cell proliferation, such as inhibiting cell proliferation of a cancer cell or cell infected with a virus. Still other embodiments described herein relate to an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA described herein for inhibiting cell proliferation, such as inhibiting cell proliferation of a cancer cell or cell infected with a virus. In some embodiments, the cancer cell is an HCC cell. In some embodiments, the cell infected with a virus is infected with hepatitis B virus.

Some embodiments described herein relate to a method of inducing apoptosis of a cell (for example, a cancer cell or cell infected with a virus) that can include contacting the cell with an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA as described herein. Other embodiments described herein relate to using an effective amount of an siRNA as described herein or a pharmaceutical composition that includes an effective amount of an siRNA in the manufacture of a medicament for inducing apoptosis of a cell, such as a cancer cell or cell infected with a virus. Still other embodiments described herein relate to the use of an effective amount of an siRNA as described herein or a pharmaceutical composition that includes an effective amount of an siRNA as described herein for inducing apoptosis of a cell, such as a cancer cell or cell infected with a virus. In some embodiments, the cancer cell is an HCC cell. In some embodiments, the cell infected with a virus is infected with hepatitis B virus.

Some embodiments described herein relate to a method of decreasing the viability of a cell (for example, a cancer cell or cell infected with a virus) that can include contacting the cell with an effective amount of an siRNA described herein, or a pharmaceutical composition that includes an effective amount of an siRNA as described herein. Other embodiments described herein relate to using an siRNA as described herein in the manufacture of a medicament for decreasing the viability of a cell, such as a cancer cell or cell infected with a virus. Still other embodiments described herein relate to the use of an effective amount of an siRNA as described herein or a pharmaceutical composition that includes an effective amount of an siRNA as described herein for decreasing the viability of a cell, such as a cancer cell or cell infected with a virus. In some embodiments, the cancer cell is an HCC cell. In some embodiments, the cell infected with a virus is infected with hepatitis B virus.

In some embodiments, the effective amount of an siRNA for a human subject is 1, 10, 50, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000 or 1, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 300, 400, 500, 600, 700, 800, 900, 1000 mg or any amount within the range defined by any two aforementioned amounts. In some embodiments, the effective amount of an siRNA for a human subject is 1, 10, 50, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000 ng/kg, or 1, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 300, 400, 500, 600, 700, 800, 900, 1000 μg/kg or any amount within the range defined by any two aforementioned amounts. In some embodiments, the effective amount of an siRNA is dosed more than one time. In some embodiments, the siRNA dose is administered every 1, 2, 3, 4, 5, 6, 7 days, or 1, 2, 3, 4 weeks, or 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 months, or 1, 2, 3, 4, 5 years, or any period or combination thereof within the range defined by any two aforementioned times. In some embodiments, at least one loading dose and at least one maintenance dose is administered to the subject, where the at least one loading dose is a higher dose of the siRNA than the at least one maintenance dose.

As used herein, the term “combination therapy” is intended to define therapies which comprise the use of a combination of two or more pharmaceutical compounds/agents or therapies. Thus, references to “combination therapy”, “combinations” and the use of compounds/agents “in combination” in this application may refer to compounds/agents that are administered as part of the same overall treatment regimen. As such, the dosage or timing of each of the two or more compounds/agents may differ: each may be administered at the same time or at different times. Accordingly, the compounds/agents of the combination may be administered sequentially (e.g. before or after) or simultaneously, either in the same pharmaceutical formulation (i.e. together), or in different pharmaceutical formulations (i.e. separately). Each of the two or more compounds/agents in a combination therapy may also differ with respect to the route of administration.

The term “inhibitor”, as used herein, refers to an enzyme inhibitor or receptor inhibitor which is a molecule that binds to an enzyme or receptor, and decreases and/or blocks its activity. The term may relate to a reversible or an irreversible inhibitor.

Cancer may be treated with surgery, radiation therapy, chemotherapy, targeted therapies, immunotherapy or hormonal therapies. Any of these mentioned therapies may be used in conjunction with another therapy as a combination therapy. Chemotherapeutic compounds include but are not limited to alemtuzumab, altretamine, azacitidine, bendamustine, bleomycin, bortezomib, busulfan, cabazitaxel, capecitabine, carboplatin, carmofur, carmustine, chlorambucil, chlormethine, cisplatin, cladribine, clofarabine, cyclophosphamide, cytarabine, dacarbazine, dactinomycin, daunorubicin, decitabine, denosumab, docetaxel, doxorubicin, epirubicin, estramustine, etoposide, everolimus, floxuridine, fludarabine, fluorouracil, fotemustine, gemcitabine, gemtuzumab, hydroxycarbamide, ibritumomab, idarubicin, ifosfamide, irinotecan, ixabepilone, lomustine, melphalan, mercaptopurine, methotrexate, mitomycin, mitoxantrone, nedaplatin, nelarabine, ofatumumab, oxaliplatin, paclitaxel, pemetrexed, pentostatin, pertuzumab, procarbazine, raltitrexed, streptozotocin, tegafur, temozolomide, temsirolimus, teniposide, tioguanine, topotecan, tositumomab, valrubicin, vinblastine, vincristine, vindesine, vinflunine, or vinorelbine, or any combination thereof.

As used herein, the term “protein kinase inhibitor” refers to inhibitors of protein kinases, serine/threonine kinases, tyrosine kinases, or dual-specificity kinases for the treatment of cancer or other illness. In some embodiments, the protein kinase inhibitor is a small molecule, compound, polysaccharide, lipid, peptide, polypeptide, protein, antibody, nucleoside, nucleoside analog, nucleotide, nucleotide analog, nucleic acid, or oligonucleotide. In some embodiments, the protein kinase inhibitor includes but is not limited to acalabrutinib, adavosertib, afatinib, alectinib, axitinib, binimetinib, bosutinib, brigatinib, cediranib, ceritinib, cetuximab, cobimetinib, crizotinib, cabozantinib, dacomitinib, dasatinib, entrectinib, erdafitinib, erlotinib, fostamatinib, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, lestaurtinib, lortatinib, masitinib, momelotinib, mubritinib, neratinib, nilotinib, nintedanib, olmutinib, osimertinib, pacritinib, panitumumab, pazopanib, pegaptanib, ponatinib, radotinib, regorafenib, rociletinib, ruxolitinib, selumetinib, semaxanib, sorafenib, sunitinib, SU6656, tivozanib, toceranib, trametinib, trastuzumab, vandetanib, or vemurafenib, or any combination thereof.

As used herein, the term “checkpoint inhibitor” refers to an immunotherapy that targets immune checkpoints to stimulate immune function. In some embodiments, the checkpoint inhibitor is a small molecule, compound, polysaccharide, lipid, peptide, polypeptide, protein, antibody, nucleoside, nucleoside analog, nucleotide, nucleotide analog, nucleic acid, or oligonucleotide. In some embodiments, the immune checkpoint is the PD-1/PD-L1 checkpoint. In some embodiments, the PD-1 checkpoint includes but is not limited to nivolumab, pembrolizumab, spartalizumab, cemiplimab, camrelizumab, sintilimab, tislelizumab, toripalimab, AMP-224 or AMP-514, or any combination thereof. In some embodiments, the PD-L1 checkpoint inhibitor includes but is not limited to atezolizumab, avelumab, durvalumab, KN035, AUNP12, CA-170, or BMS-986189, or any combination thereof. In some embodiments, the immune checkpoint is the CTLA-4 checkpoint. In some embodiments, the CTLA-4 checkpoint inhibitor includes but is not limited to ipilimumab or tremilimumab, or any combination thereof.

As used herein, the term “VEGF inhibitor” refers to inhibitors of vascular endothelial growth factor (VEGF) or a VEGF receptor (VEGFR). In some embodiments, the VEGF inhibitor is a small molecule, compound, polysaccharide, lipid, peptide, polypeptide, protein, antibody, nucleoside, nucleoside analog, nucleotide, nucleotide analog, nucleic acid, or oligonucleotide. In some embodiments, the VEGF inhibitor includes but is not limited to aflibercept, axitinib, bevacizumab, brivanib, cabozantinib, cediranib, lenvatinib, linifinib, nintedanib, pazopanib, ponatinib, ramucirumab, regorafenib, semaxanib, sorafenib, sunitinib, tivozanib, toceranib, or vandetanib, or any combination thereof.

As used herein, the term “antiviral medication” refers to a pharmaceutical composition administered to treat a viral infection. In some embodiments, the viral infection is caused by adenovirus, Ebola virus, coronavirus, Epstein-Barr virus (EBV), Friend virus, hantavirus, hepatitis B virus (HBV), hepatitis C virus (HCV), herpes simplex virus, human immunodeficiency virus (HIV), human metapneumovirus, human papillomavirus (HPV), influenza virus, Japanese encephalitis virus, Kaposi's sarcoma-associated herpesvirus, lymphocytic choriomeningitis virus, parainfluenza virus, rabies virus, respiratory syncytial virus, rhinovirus, varicella zoster virus. In some embodiments, the antiviral medication is a small molecule, compound, polysaccharide, lipid, peptide, polypeptide, protein, antibody, nucleoside, nucleoside analog, nucleotide, nucleotide analog, nucleic acid, or oligonucleotide. In some embodiments, the antiviral medication is an interferon, a capsid assembly modulator, a sequence specific oligonucleotide, an entry inhibitor, or a small molecule immunomodulatory. In some embodiments, the antiviral medication includes but is not limited to AB-423, AB-506, ABI-H2158, ABI-H0731, acyclovir, adapromine, adefovir, alafenamide, amantadine, asunaprevir, baloxavir marboxil, beclabuvir, boceprevir, brivudine, cidofovir, ciluprevir, clevudine, cytarabine, daclatasvir, danoprevir, dasabuvir, deleobuvir, dipivoxil, edoxudine, elbasvir, entecavir, faldaprevir, famciclovir, favipiravir, filibuvir, fomivirsen, foscarnet, galidesivir, ganciclovir, glecaprevir, GLS4, grazoprevir, idoxuridine, imiquimod, IFN-α, interferon alfa 2b, JNJ-440, JNJ-6379, lamivudine, laninamivir, ledipasvir, mericitabine, methisazone, MK-608, moroxydine, narlaprevir, NITD008, NZ-4, odalasvir, ombitasvir, oseltamivir, paritaprevir, peginterferon alfa-2a, penciclovir, peramivir, pibrentasvir, pimodivir, pleconaril, podophyllotoxin, presatovir, radalbuvir, ravidasvir, remdesivir, REP 2139, REP 2165, resiquimod, RG7907, ribavirin, rifampicin, rimantadine, ruzasvir, samatasvir, setrobuvir, simeprevir, sofosbuvir, sorivudine, sovaprevir, taribavirin, telaprevir, telbivudine, tenofovir, tenofovir disoproxil, triazavirin, trifluridine, tromantadine, umifenovir, uprifosbuvir, valaciclovir, valgancicovir, vaniprevir, vedroprevir, velpatasvir, vidarabine, voxilaprevir, or zanamivir, or any combination thereof.

The term “% w/w” or “% wt/wt” as used herein has its ordinary meaning as understood in light of the specification and refers to a percentage expressed in terms of the weight of the ingredient or agent over the total weight of the composition multiplied by 100. The term “% v/v” or “% vol/vol” as used herein has its ordinary meaning as understood in the light of the specification and refers to a percentage expressed in terms of the liquid volume of the compound, substance, ingredient, or agent over the total liquid volume of the composition multiplied by 100.

The invention is generally disclosed herein using affirmative language to describe the numerous embodiments. The invention also includes embodiments in which subject matter is excluded, in full or in part, such as substances or materials, method steps and conditions, protocols, or procedures.

EXAMPLES

Some aspects of the embodiments discussed above are disclosed in further detail in the following examples, which are not in any way intended to limit the scope of the present disclosure. Those in the art will appreciate that many other embodiments also fall within the scope of the invention, as it is described herein above and in the claims.

Example 1: siRNA Design

siRNAs of 18-21 nucleotides in length were selected. Mismatches were allowed only outside of the seed region on the antisense strand, as shown in Table 7. The seed region is in positions 2-8, with the position numbering based on the antisense strand. The strand length excludes the two nucleotide overhang.

TABLE 7 Allowed mismatch positions in siRNAs Fully conserved Allowed siRNA Maximum positions mismatch length mismatches (seed region) positions 18 2 2-8 1, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18 19 2 2-8 1, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 20 2 2-8 1, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 21 2 2-8 1, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21

Example 2: siRNAs Targeting the Human CD274 Gene (PD-L1)

siRNAs were designed using the human CD274 mRNA transcript (NCBI accession number NM_014143.4, 3634 nt in length, SEQ ID NO: 1) as the template. 18-mers are listed in Table 8 (SEQ ID NOs: 2-93). 19-mers are depicted in Table 9 (SEQ ID NOs: 94-167 and 283-380). 20-mers are depicted in Table 10 (SEQ ID NOs: 168-229). 21-mers are depicted in Table 11 (SEQ ID NOs: 230-282). All of the listed siRNAs depict the antisense strand. Sense strands (which are not listed) are perfectly complementary to each listed antisense strand.

Any of the siRNAs listed herein, and the individual nucleobases, sugars, linkages, nucleosides, nucleotides and additional moieties thereof, can be constructed and used with any of the modifications described herein. The sequences listed in Tables 8-11 and SEQ ID NOs: 2-380 represent the unmodified oligonucleotide sequence prior to application of modifications.

TABLE 8 CD274 siRNAs-18-mers Target Target start positions siRNA Antisense SEQ position spanned Strand Sequence ID NO:   69 86-69 ACAGCAAATATCCTCATC  2   70 87-70 GACAGCAAATATCCTCAT  3   71 88-71 AGACAGCAAATATCCTCA  4   72 89-72 AAGACAGCAAATATCCTC  5   73 90-73 AAAGACAGCAAATATCCT  6   74 91-74 TAAAGACAGCAAATATCC  7   75 92-75 ATAAAGACAGCAAATATC  8   76 93-76 TATAAAGACAGCAAATAT  9   77 94-77 ATATAAAGACAGCAAATA 10   78 95-78 AATATAAAGACAGCAAAT 11 1398 1415-1398 AGACTCAAAATAAATAGG 12 1399 1416-1399 CAGACTCAAAATAAATAG 13 1400 1417-1400 ACAGACTCAAAATAAATA 14 1401 1418-1401 CACAGACTCAAAATAAAT 15 1402 1419-1402 TCACAGACTCAAAATAAA 16 1403 1420-1403 CTCACAGACTCAAAATAA 17 1404 1421-1404 CCTCACAGACTCAAAATA 18 1405 1422-1405 ACCTCACAGACTCAAAAT 19 1406 1423-1406 GACCTCACAGACTCAAAA 20 1407 1424-1407 AGACCTCACAGACTCAAA 21 2700 2717-2700 ATAACTTAGAAACAAAGA 22 2701 2718-2701 GATAACTTAGAAACAAAG 23 2702 2719-2702 AGATAACTTAGAAACAAA 24  277 294-277 CTTCAGGTCTTCCTCTCC 25 3038 3055-3038 GGTAGCTAGCAGTCAAGG 26 3039 3056-3039 GGGTAGCTAGCAGTCAAG 27 3040 3057-3040 AGGGTAGCTAGCAGTCAA 28 3041 3058-3041 CAGGGTAGCTAGCAGTCA 29 3239 3256-3239 TTCAGCCTTGACATGTGG 30 3240 3257-3240 CTTCAGCCTTGACATGTG 31 3241 3258-3241 TCTTCAGCCTTGACATGT 32 3242 3259-3242 TTCTTCAGCCTTGACATG 33 3243 3260-3243 TTTCTTCAGCCTTGACAT 34  350 367-350 GAAGTGCAGCATTTCCCA 35  351 368-351 TGAAGTGCAGCATTTCCC 36  352 369-352 CTGAAGTGCAGCATTTCC 37 3527 3544-3527 TTTATTAAATTAATGCAG 38 3528 3545-3528 TTTTATTAAATTAATGCA 39 3529 3546-3529 ATTTTATTAAATTAATGC 40  353 370-353 TCTGAAGTGCAGCATTTC 41  354 371-354 ATCTGAAGTGCAGCATTT 42 3542 3559-3542 AATAAATAAGAATATTTT 43  355 372-355 GATCTGAAGTGCAGCATT 44  363 380-363 ACATCTGTGATCTGAAGT 45  364 381-364 CACATCTGTGATCTGAAG 46  365 382-365 TCACATCTGTGATCTGAA 47  366 383-366 TTCACATCTGTGATCTGA 48  414 431-414 GCACCACCATAGCTGATC 49  415 432-415 GGCACCACCATAGCTGAT 50  423 440-423 TTGTAGTCGGCACCACCA 51  424 441-424 CTTGTAGTCGGCACCACC 52  432 449-432 GTAATTCGCTTGTAGTCG 53  433 450-433 AGTAATTCGCTTGTAGTC 54  451 468-451 TGGGGCATTGACTTTCAC 55  452 469-452 ATGGGGCATTGACTTTCA 56  453 470-453 TATGGGGCATTGACTTTC 57  454 471-454 GTATGGGGCATTGACTTT 58  455 472-455 TGTATGGGGCATTGACTT 59  456 473-456 TTGTATGGGGCATTGACT 60  457 474-457 GTTGTATGGGGCATTGAC 61  458 475-458 TGTTGTATGGGGCATTGA 62  459 476-459 TTGTTGTATGGGGCATTG 63  460 477-460 TTTGTTGTATGGGGCATT 64  461 478-461 TTTTGTTGTATGGGGCAT 65  462 479-462 ATTTTGTTGTATGGGGCA 66  463 480-463 GATTTTGTTGTATGGGGC 67  464 481-464 TGATTTTGTTGTATGGGG 68  473 490-473 TTCTTTGGTTGATTTTGT 69  474 491-474 ATTCTTTGGTTGATTTTG 70  475 492-475 AATTCTTTGGTTGATTTT 71  476 493-476 AAATTCTTTGGTTGATTT 72  477 494-477 AAAATTCTTTGGTTGATT 73  499 516-499 AGAGGTGACTGGATCCAC 74  500 517-500 CAGAGGTGACTGGATCCA 75  501 518-501 TCAGAGGTGACTGGATCC 76  520 537-520 CTGACATGTCAGTTCATG 77  531 548-531 TAGCCCTCAGCCTGACAT 78  564 581-564 TCACTGCTTGTCCAGATG 79  565 582-565 GTCACTGCTTGTCCAGAT 80  566 583-566 GGTCACTGCTTGTCCAGA 81  567 584-567 TGGTCACTGCTTGTCCAG 82  641 658-641 GTGTGCTGGTCACATTGA 83  642 659-642 AGTGTGCTGGTCACATTG 84  643 660-643 CAGTGTGCTGGTCACATT 85  644 661-644 TCAGTGTGCTGGTCACAT 86  645 662-645 CTCAGTGTGCTGGTCACA 87  742 759-742 AGGTAGTTCTGGGATGAC 88  743 760-743 GAGGTAGTTCTGGGATGA 89  893 910-893 TCTTTGAGTTTGTATCTT 90  894 911-894 TTCTTTGAGTTTGTATCT 91  918 935-918 TCCTCCAAATGTGTATCA 92  919 936-919 CTCCTCCAAATGTGTATC 93

TABLE 9 CD274 siRNAs-19mers Target Target start positions siRNA Antisense SEQ position spanned Strand Sequence ID NO:   69  87-69 GACAGCAAATATCCTCATC  94   70  88-70 AGACAGCAAATATCCTCAT  95   71  89-71 AAGACAGCAAATATCCTCA  96   72  90-72 AAAGACAGCAAATATCCTC  97   73  91-73 TAAAGACAGCAAATATCCT  98   74  92-74 ATAAAGACAGCAAATATCC  99   75  93-75 TATAAAGACAGCAAATATC 100   76  94-76 ATATAAAGACAGCAAATAT 101   77  95-77 AATATAAAGACAGCAAATA 102   78  96-78 GAATATAAAGACAGCAAAT 103 1398  1416-1398 CAGACTCAAAATAAATAGG 104 1399  1417-1399 ACAGACTCAAAATAAATAG 105 1400  1418-1400 CACAGACTCAAAATAAATA 106 1401  1419-1401 TCACAGACTCAAAATAAAT 107 1402  1420-1402 CTCACAGACTCAAAATAAA 108 1403  1421-1403 CCTCACAGACTCAAAATAA 109 1404  1422-1404 ACCTCACAGACTCAAAATA 110 1405  1423-1405 GACCTCACAGACTCAAAAT 111 1406  1424-1406 AGACCTCACAGACTCAAAA 112 2700  2718-2700 GATAACTTAGAAACAAAGA 113 2701  2719-2701 AGATAACTTAGAAACAAAG 114 3038  3056-3038 GGGTAGCTAGCAGTCAAGG 115 3039  3057-3039 AGGGTAGCTAGCAGTCAAG 116 3040  3058-3040 CAGGGTAGCTAGCAGTCAA 117 3239  3257-3239 CTTCAGCCTTGACATGTGG 118 3240  3258-3240 TCTTCAGCCTTGACATGTG 119 3241  3259-3241 TTCTTCAGCCTTGACATGT 120 3242  3260-3242 TTTCTTCAGCCTTGACATG 121 3243  3261-3243 GTTTCTTCAGCCTTGACAT 122  350  368-350 TGAAGTGCAGCATTTCCCA 123  351  369-351 CTGAAGTGCAGCATTTCCC 124  352  370-352 TCTGAAGTGCAGCATTTCC 125 3527  3545-3527 TTTTATTAAATTAATGCAG 126 3528  3546-3528 ATTTTATTAAATTAATGCA 127  353  371-353 ATCTGAAGTGCAGCATTTC 128  354  372-354 GATCTGAAGTGCAGCATTT 129  355  373-355 TGATCTGAAGTGCAGCATT 130  364  382-364 TCACATCTGTGATCTGAAG 131  365  383-365 TTCACATCTGTGATCTGAA 132  415  433-415 CGGCACCACCATAGCTGAT 133  423  441-423 CTTGTAGTCGGCACCACCA 134  424  442-424 GCTTGTAGTCGGCACCACC 135  451  469-451 ATGGGGCATTGACTTTCAC 136  452  470-452 TATGGGGCATTGACTTTCA 137  453  471-453 GTATGGGGCATTGACTTTC 138  454  472-454 TGTATGGGGCATTGACTTT 139  455  473-455 TTGTATGGGGCATTGACTT 140  456  474-456 GTTGTATGGGGCATTGACT 141  457  475-457 TGTTGTATGGGGCATTGAC 142  458  476-458 TTGTTGTATGGGGCATTGA 143  459  477-459 TTTGTTGTATGGGGCATTG 144  460  478-460 TTTTGTTGTATGGGGCATT 145  461  479-461 ATTTTGTTGTATGGGGCAT 146  462  480-462 GATTTTGTTGTATGGGGCA 147  463  481-463 TGATTTTGTTGTATGGGGC 148  464  482-464 TTGATTTTGTTGTATGGGG 149  473  491-473 ATTCTTTGGTTGATTTTGT 150  474  492-474 AATTCTTTGGTTGATTTTG 151  475  493-475 AAATTCTTTGGTTGATTTT 152  476  494-476 AAAATTCTTTGGTTGATTT 153  499  517-499 CAGAGGTGACTGGATCCAC 154  500  518-500 TCAGAGGTGACTGGATCCA 155  520  538-520 CCTGACATGTCAGTTCATG 156  564  582-564 GTCACTGCTTGTCCAGATG 157  565  583-565 GGTCACTGCTTGTCCAGAT 158  566  584-566 TGGTCACTGCTTGTCCAGA 159  567  585-567 ATGGTCACTGCTTGTCCAG 160  641  659-641 AGTGTGCTGGTCACATTGA 161  642  660-642 CAGTGTGCTGGTCACATTG 162  643  661-643 TCAGTGTGCTGGTCACATT 163  644  662-644 CTCAGTGTGCTGGTCACAT 164  893  911-893 TTCTTTGAGTTTGTATCTT 165  918  936-918 CTCCTCCAAATGTGTATCA 166  919  937-919 TCTCCTCCAAATGTGTATC 167   23  41-23 AAGCGCGGCTGGTGCGGAG 283   43  61-43 AATGCCCTGCAGGCGGACA 284  103  121-103 CGTTCAGCAAATGCCAGTA 285  123  141-123 GGGAACCGTGACAGTAAAT 286  143  161-143 TCTACCACATATAGGTCCT 287  163  181-163 TTGTCATATTGCTACCATA 288  183  201-183 TACTGGGAATTTGCATTCA 289  203  221-203 GCCAGGTCTAATTGTTTTT 290  223  241-223 CCCAATAGACAATTAGTGC 291  263  281-263 TCTCCATGCACAAATTGAA 292  283  301-283 GCTGAACCTTCAGGTCTTC 293  303  321-303 CCTCTGTCTGTAGCTACTA 294  323  341-323 TGGTCCTTCAACAGCCGGG 295  543  561-543 TTCGGCCTTGGGGTAGCCC 296  603  621-603 GGAATTGGTGGTGGTGGTC 297  723  741-723 CAATTCAGCTGTATGGTTT 298  763  781-763 TTTCATTTGGAGGATGTGC 299  803  821-803 AGGCATAATAAGATGGCTC 300  823  841-823 TGAATGTCAGTGCTACACC 301  843  861-843 CCCTTTTCTTAAACGGAAG 302  863  881-863 TTTTTCACATCCATCATTC 303  963  981-963 GAGAATCCCTGCTTGAAGA 304  983 1001-983 GAACCCCTAAACCACAGGT 305 1063  1081-1063 TCAGTGCTTGGGCCTTTTA 306 1083  1101-1083 GCTTTCGCCAGGTTCCATT 307 1183  1201-1183 CCCTGTCACAGGCGTCGAT 308 1203  1221-1203 TGTTCAGAAGTATCCTTTC 309 1263  1281-1263 TTAGGGATTCTCAACCCGT 310 1283  1301-1283 TGCAGGAACTGACCCTCAA 311 1323  1341-1323 AAAACAAATTGAGGCATTG 312 1363  1381-1363 ATACTGTCCCGTTCCAACA 313 1443  1461-1443 AAAAGAAATCATTCACAAC 314 1483  1501-1483 TTTGGCGACAAAATTGTAA 315 1503  1521-1503 TCATTAAGCAGCAAGTTTA 316 1543  1561-1543 CACCTTACAAATACTCCAT 317 1583  1601-1583 ATGCTTCCAATGTATACTT 318 1603  1621-1603 CAACCAACGGTTTGATCTT 319 1623  1641-1623 AATAAAGGTGACATCCTAT 320 1683  1701-1683 ACTGCACAGACACTTGAGG 321 1703  1721-1703 GATATTTAAATGGAACAGA 322 1723  1741-1723 TACCACATAATTGTAAAGC 323 1743  1761-1743 ATGAGATTATGTGTGTAGG 324 1843  1861-1843 ATTTACTGGTTTGGGCAAG 325 1863  1881-1863 GTGGCAGTCTGAGGTCTGC 326 1883  1901-1883 GTATTATAAAAGGACAGTG 327 1903  1921-1903 GTAAAATATAGCTGTAAAT 328 1923  1941-1923 GAATAAAAGAATTGCTTAA 329 1943  1961-1943 GCACTTAATAAATGGTTTT 330 1963  1981-1963 CAGCGATTGATATTGCAAG 331 2003  2021-2003 TACTTTGTCTTGCTCACAT 332 2043  2061-2043 GTTAATCTCCTCATTATAC 333 2083  2101-2083 TGCTATGACACTGGACTAA 334 2123  2141-2123 TTGGCAACACTGCTCGGGT 335 2163  2181-2163 TATCCAACCGTCCCAGACC 336 2203  2221-2203 TGTAAATGAAAATTACTCT 337 2223  2241-2223 TTTAAGTACCGACCTCTCT 338 2263  2281-2263 ATGCTAGAAAAGGAATTCC 339 2283  2301-2283 GCAAATCAGGAATAAATAT 340 2323  2341-2323 CCAGACACTATATAAACAA 341 2343  2361-2343 GACAGAACTGTTAAACAAT 342 2383  2401-2383 AAGGTATGAATTTAAAATT 343 2423  2441-2423 AACCATCTCCCATGGGATC 344 2443  2461-2443 GGATGAAGTGGAGATTTTC 345 2463  2481-2463 GGAAACTTGAATGGCTTGG 346 2483  2501-2483 GTAGCAGTTGCTTCTGGAA 347 2503  2521-2503 GAACATATGAATGAAAGGC 348 2563  2581-2563 AAAAAATTTTAAAAATACG 349 2583  2601-2583 CAATGTGTTACTATTTAGG 350 2643  2661-2643 CCATCTGCTATATAAGAAA 351 2663  2681-2663 CTGGGAACTTCAAATTCAT 352 2723  2741-2723 AGATAATGAAAAGCTATGG 353 2743  2761-2743 CATATACTGGATCATATGA 354 2763  2781-2763 TATATGTAGGACATATTTA 355 2783  2801-2783 AAATGGTGGTTGTCTAAAT 356 2803  2821-2803 TCCTAGAGCAAATACTTAA 357 2823  2841-2823 ATAAACAAATCCAAACTCT 358 2863  2881-2863 GTGCACCCTGGAGAGCCCA 359 2883  2901-2883 TTTAGGACTAGATTGACTC 360 2903  2921-2903 AGTTAATAATAAGATTGCT 361 2923  2941-2923 GACATGATTCTGTCATACA 362 2943  2961-2943 AGCAGAAAACAAAAGTTCC 363 2983  3001-2983 TGCAAGTACAGCATCAAAG 364 3003  3021-3003 CCAGAAAGAAAATGTGATT 365 3063  3081-3063 CAACGAATGAGGCTTTTCT 366 3083  3101-3083 GGCATTCAAGGGTTCAAGC 367 3103  3121-3103 GTGTAGTGATGACAGCTGG 368 3183  3201-3183 TGGCCAAGAGGGAAAGGAA 369 3203  3221-3203 TTGTCATTGACACCAGAAT 370 3263  3281-3263 GGAGCTCTGTTGGAGACAC 371 3283  3301-3283 TGTACAAACAGATAACACA 372 3323  3341-3323 ACAAAGAACACTGTCACAC 373 3343  3361-3343 AATTCTTGCCTGTAATTCA 374 3383  3401-3383 TAGGAATAGACTGAGTAGA 375 3423  3441-3423 GTGCCTTACAAATCCAACA 376 3443  3461-3443 CATGAGACAAAAGGGATAA 377 3463  3481-3463 CTATGCCATTTACGATGAA 378 3563  3581-3563 ATGCTGGTGTACCAAGTAA 379 3603  3621-3603 TGAACATTTTATTAAACAC 380

TABLE 10 CD274 siRNAs-20mers Target Target start positions siRNA Antisense SEQ position spanned Strand Sequence ID NO:   70 89-70 AAGACAGCAAATATCCTCAT 168   71 90-71 AAAGACAGCAAATATCCTCA 169   72 91-72 TAAAGACAGCAAATATCCTC 170   73 92-73 ATAAAGACAGCAAATATCCT 171   74 93-74 TATAAAGACAGCAAATATCC 172   75 94-75 ATATAAAGACAGCAAATATC 173   76 95-76 AATATAAAGACAGCAAATAT 174   77 96-77 GAATATAAAGACAGCAAATA 175   78 97-78 TGAATATAAAGACAGCAAAT 176 1398 1417-1398 ACAGACTCAAAATAAATAGG 177 1399 1418-1399 CACAGACTCAAAATAAATAG 178 1400 1419-1400 TCACAGACTCAAAATAAATA 179 1401 1420-1401 CTCACAGACTCAAAATAAAT 180 1402 1421-1402 CCTCACAGACTCAAAATAAA 181 1403 1422-1403 ACCTCACAGACTCAAAATAA 182 1404 1423-1404 GACCTCACAGACTCAAAATA 183 1405 1424-1405 AGACCTCACAGACTCAAAAT 184 2700 2719-2700 AGATAACTTAGAAACAAAGA 185 3038 3057-3038 AGGGTAGCTAGCAGTCAAGG 186 3039 3058-3039 CAGGGTAGCTAGCAGTCAAG 187 3240 3259-3240 TTCTTCAGCCTTGACATGTG 188 3241 3260-3241 TTTCTTCAGCCTTGACATGT 189 3242 3261-3242 GTTTCTTCAGCCTTGACATG 190 3243 3262-3243 TGTTTCTTCAGCCTTGACAT 191  350 369-350 CTGAAGTGCAGCATTTCCCA 192  351 370-351 TCTGAAGTGCAGCATTTCCC 193  352 371-352 ATCTGAAGTGCAGCATTTCC 194  353 372-353 GATCTGAAGTGCAGCATTTC 195  354 373-354 TGATCTGAAGTGCAGCATTT 196  355 374-355 GTGATCTGAAGTGCAGCATT 197  364 383-364 TTCACATCTGTGATCTGAAG 198  415 434-415 TCGGCACCACCATAGCTGAT 199  423 442-423 GCTTGTAGTCGGCACCACCA 200  424 443-424 CGCTTGTAGTCGGCACCACC 201  451 470-451 TATGGGGCATTGACTTTCAC 202  452 471-452 GTATGGGGCATTGACTTTCA 203  453 472-453 TGTATGGGGCATTGACTTTC 204  454 473-454 TTGTATGGGGCATTGACTTT 205  455 474-455 GTTGTATGGGGCATTGACTT 206  456 475-456 TGTTGTATGGGGCATTGACT 207  457 476-457 TTGTTGTATGGGGCATTGAC 208  458 477-458 TTTGTTGTATGGGGCATTGA 209  459 478-459 TTTTGTTGTATGGGGCATTG 210  460 479-460 ATTTTGTTGTATGGGGCATT 211  461 480-461 GATTTTGTTGTATGGGGCAT 212  462 481-462 TGATTTTGTTGTATGGGGCA 213  463 482-463 TTGATTTTGTTGTATGGGGC 214  464 483-464 GTTGATTTTGTTGTATGGGG 215  473 492-473 AATTCTTTGGTTGATTTTGT 216  474 493-474 AAATTCTTTGGTTGATTTTG 217  475 494-475 AAAATTCTTTGGTTGATTTT 218  499 518-499 TCAGAGGTGACTGGATCCAC 219  520 539-520 GCCTGACATGTCAGTTCATG 220  564 583-564 GGTCACTGCTTGTCCAGATG 221  565 584-565 TGGTCACTGCTTGTCCAGAT 222  566 585-566 ATGGTCACTGCTTGTCCAGA 223  567 586-567 GATGGTCACTGCTTGTCCAG 224  641 660-641 CAGTGTGCTGGTCACATTGA 225  642 661-642 TCAGTGTGCTGGTCACATTG 226  643 662-643 CTCAGTGTGCTGGTCACATT 227  918 937-918 TCTCCTCCAAATGTGTATCA 228  919 938-919 GTCTCCTCCAAATGTGTATC 229

TABLE 11 CD274 siRNAs-21mers Target Target start positions siRNA Antisense SEQ position spanned Strand Sequence ID NO:   70 90-70 AAAGACAGCAAATATCCTCAT 230   71 91-71 TAAAGACAGCAAATATCCTCA 231   72 92-72 ATAAAGACAGCAAATATCCTC 232   73 93-73 TATAAAGACAGCAAATATCCT 233   74 94-74 ATATAAAGACAGCAAATATCC 234   75 95-75 AATATAAAGACAGCAAATATC 235   76 96-76 GAATATAAAGACAGCAAATAT 236   77 97-77 TGAATATAAAGACAGCAAATA 237 1398 1418-1398 CACAGACTCAAAATAAATAGG 238 1399 1419-1399 TCACAGACTCAAAATAAATAG 239 1400 1420-1400 CTCACAGACTCAAAATAAATA 240 1401 1421-1401 CCTCACAGACTCAAAATAAAT 241 1402 1422-1402 ACCTCACAGACTCAAAATAAA 242 1403 1423-1403 GACCTCACAGACTCAAAATAA 243 1404 1424-1404 AGACCTCACAGACTCAAAATA 244 3038 3058-3038 CAGGGTAGCTAGCAGTCAAGG 245 3240 3260-3240 TTTCTTCAGCCTTGACATGTG 246 3241 3261-3241 GTTTCTTCAGCCTTGACATGT 247 3242 3262-3242 TGTTTCTTCAGCCTTGACATG 248 3243 3263-3243 CTGTTTCTTCAGCCTTGACAT 249  350 370-350 TCTGAAGTGCAGCATTTCCCA 250  351 371-351 ATCTGAAGTGCAGCATTTCCC 251  352 372-352 GATCTGAAGTGCAGCATTTCC 252  353 373-353 TGATCTGAAGTGCAGCATTTC 253  354 374-354 GTGATCTGAAGTGCAGCATTT 254  355 375-355 TGTGATCTGAAGTGCAGCATT 255  415 435-415 GTCGGCACCACCATAGCTGAT 256  423 443-423 CGCTTGTAGTCGGCACCACCA 257  424 444-424 TCGCTTGTAGTCGGCACCACC 258  451 471-451 GTATGGGGCATTGACTTTCAC 259  452 472-452 TGTATGGGGCATTGACTTTCA 260  453 473-453 TTGTATGGGGCATTGACTTTC 261  454 474-454 GTTGTATGGGGCATTGACTTT 262  455 475-455 TGTTGTATGGGGCATTGACTT 263  456 476-456 TTGTTGTATGGGGCATTGACT 264  457 477-457 TTTGTTGTATGGGGCATTGAC 265  458 478-458 TTTTGTTGTATGGGGCATTGA 266  459 479-459 ATTTTGTTGTATGGGGCATTG 267  460 480-460 GATTTTGTTGTATGGGGCATT 268  461 481-461 TGATTTTGTTGTATGGGGCAT 269  462 482-462 TTGATTTTGTTGTATGGGGCA 270  463 483-463 GTTGATTTTGTTGTATGGGGC 271  464 484-464 GGTTGATTTTGTTGTATGGGG 272  473 493-473 AAATTCTTTGGTTGATTTTGT 273  474 494-474 AAAATTCTTTGGTTGATTTTG 274  564 584-564 TGGTCACTGCTTGTCCAGATG 275  565 585-565 ATGGTCACTGCTTGTCCAGAT 276  566 586-566 GATGGTCACTGCTTGTCCAGA 277  567 587-567 TGATGGTCACTGCTTGTCCAG 278  641 661-641 TCAGTGTGCTGGTCACATTGA 279  642 662-642 CTCAGTGTGCTGGTCACATTG 280  918 938-918 GTCTCCTCCAAATGTGTATCA 281  919 939-919 CGTCTCCTCCAAATGTGTATC 282

Example 3: Treatment of Cancer Using CD274 siRNAs

A human patient presents with a cancer, such as a hepatocellular carcinoma (HCC). The cancer is a non-metastatic or metastatic cancer. In the case of HCC, the patient may also have another liver condition, such as fibrosis, cirrhosis, non-alcoholic liver disease, hepatitis, hepatitis B, or hepatitis C. An effective amount of a CD274 siRNA or a pharmaceutical composition comprising an effective amount of a CD274 siRNA is administered to the patient parenterally. The CD274 siRNA is selected from the group consisting of SEQ ID NOs: 2-380, including any allowed mismatches as described herein. The CD274 siRNA can optionally have any of the modifications to individual nucleobases, sugars, linkages, nucleosides, or nucleotides as described herein. The CD274 siRNA can also optionally have a covalently conjugated targeting moiety to improve selectivity to tumor and/or liver tissue. The CD274 siRNA can be constructed of deoxyribose sugars (DNA nucleotides), ribose sugars (RNA nucleotides) or any combination thereof. The CD274 siRNA can be constructed of unmodified nucleotides or modified nucleotides or any combination thereof. The CD274 siRNA or pharmaceutical composition comprising the CD274 siRNA can optionally be administered as a combination therapy with another anti-neoplastic compound or therapy.

Following administration of an effective amount of the CD274 siRNA or the pharmaceutical composition comprising an effective amount of the CD274 siRNA, the cancer is reduced or eliminated.

Example 4: Treatment of Hepatitis B Using CD274 siRNAs

A human patient presents with a hepatitis B infection. The hepatitis B infection is acute or chronic. The hepatitis B infection may also be coincidental with a hepatitis D infection. The patient may also have another liver conditions, such as fibrosis, cirrhosis, non-alcoholic liver disease, or HCC. An effective amount of a CD274 siRNA or a pharmaceutical composition comprising an effective amount of a CD274 siRNA is administered to the patient parenterally. The CD274 siRNA is selected from the group consisting of SEQ ID NOs: 2-380. The CD274 siRNA can optionally have any of the modifications to individual nucleobases, sugars, linkages, nucleosides, or nucleotides as described herein. The CD274 siRNA can also optionally have a covalently conjugated targeting moiety to improve selectivity to liver tissue. The CD274 siRNA can be constructed of deoxyribose sugars (DNA nucleotides), ribose sugars (RNA nucleotides) or any combination thereof. The CD274 siRNA can be constructed of unmodified nucleotides or modified nucleotides or any combination thereof. The CD274 siRNA or pharmaceutical composition comprising the CD274 siRNA can optionally be administered as a combination therapy with another antiviral medication.

Following administration of an effective amount of the CD274 siRNA or the pharmaceutical composition comprising an effective amount of the CD274 siRNA, the hepatitis B infection (and optionally, hepatitis D infection) is reduced or eliminated.

Example 5: Treatment of Hepatocellular Carcinoma Cells Using siRNAs

Human hepatocellular carcinoma cells (SNU-387) were seeded at 30,000 cells/well in a 96-well plate. The siRNAs, including any of SEQ ID NOs: 2-380, were transfected with Lipofectamine RNAiMax (Life Technologies) in the seeded SNU-387 cells. The siRNAs included any of the modifications described herein, including modification of individual nucleobases, sugars, linkages, nucleosides, or nucleotides. The modifications of the siRNAs varied across different sequences. For example, in some sequences, such as SEQ ID NOs: 94-167 (19-mers), the sense strand included purines as 2′OMe and pyrimidines as 2′F, with two nucleotide overhang at the 3′-end, which are two mU nucleotides. All linkages in the modified SEQ ID NOs: 94-167 sense strand included phosphodiester (PO) linkages, except for the two most 5′- and 3′-end linkages, which were phosphorothioate (PS), for a total of four PS linkages. In addition, the antisense strands for SEQ ID NOs: 94-167 and 283-380 (19-mers) included alternating 2′OMe and 2′F pattern, starting with 2′OMe at the 5′ end, with two nucleotide overhang at the 3′-end, which are two mU nucleotides. All linkages in the modified SEQ ID NOs: 94-167 antisense strand included PO linkages, except for the two most 5′- and 3′-end linkages, which were PS linkages, for a total of four PS linkages.

As another example, in some sequences, such as in SEQ ID NOs: 283-380 (19-mers), the sense strand included alternating 2′OMe and 2′F pattern, starting with 2′F at the 5′ end, with two nucleotide overhang at the 3′-end, which are two mU nucleotides. All linkages in the modified SEQ ID NOs: 283-380 sense strand included phosphodiester (PO) linkages, except for the two most 5′- and 3′-end linkages, which were phosphorothioate (PS), for a total of four PS linkages. In addition, the antisense strands for SEQ ID NOs: 283-380 (19-mers) included alternating 2′OMe and 2′F pattern, starting with 2′OMe at the 5′ end, with two nucleotide overhang at the 3′-end, which are two mU nucleotides. All linkages in the modified SEQ ID NOs: 283-380 antisense strand included PO linkages, except for the two most 5′- and 3′-end linkages, which were PS linkages, for a total of four PS linkages.

As another example, in some sequences, such as in SEQ ID NOs: 230-282 (21-mers), the sense strand included purines as 2′OMe and pyrimidines as 2′F, with all linkages as PO, except for the two most 5′-end linkages, which were PS linkages, for a total of two PS linkages. The sense strand in these 21-mer sequences did not include an overhang, but were blunt ended. The antisense strand for SEQ ID NOs: 230-282 (21-mers) included alternating 2′OMe and 2′F pattern, starting with 2′OMe at the 5′end, with a two nucleotide overhang at the 3′-end, which were two mU nucleotides. All linkages in the 21-mer antisense strands were PO linkages, except for the two most 5′- and 3′-end linkages, which were PS linkages, for a total of four PS linkages. It is to be understood that these modifications to these sequences are exemplary, and that any modifications as described herein on any siRNA sequence can be employed.

For dose response curves, a 4-fold dilution series of siRNA (top dose 50 nM; 6 concentrations tested total) was tested. At 48 hr post transfection, cells were harvested, RNA was extracted with RNeasy 96 Kits (Qiagen), and RT-qPCR is performed to assess PD-L1 gene knockdown. Cell viability (of separate plate treated the same way) was assessed at 48 h post transfection using Cell Titer Glo (Promega); protocol according to manufacturer's instructions. Data was fit with GraphPad Prism using a four parameter dose response equation. Table 12 provides representative EC50 and CC50 values for selected siRNA. FIG. 1 depicts the fraction of PD-L1 mRNA remaining.

TABLE 12 Relative Gene Expression for select siRNA sequences SEQ ID NO: EC50 (nM) CC50 (nM) 106 A X 125 C X 134 B X 127 C X A < 0.4 nM; B = 0.4-0.8 nM; C > 0.8-1.2 nM X > 50 nM; Y ≤ 50 nM

In a separate experiment, the siRNA were transfected with Lipofectamine RNAiMax (Life Technologies) in SNU-387 cells, seeded at 30,000 cells/well in 96-well plates. Two concentrations were tested (20 and 0.2 nM) for each siRNA. At 48 hr post transfection, cells were harvested, RNA was extracted with RNeasy 96 Kits (Qiagen), and RT-qPCR was performed to assess PD-L1 gene knockdown. Cell viability (of separate plate treated the same way) was assessed at 48 h post transfection using Cell Titer Glo (Promega); protocol according to manufacturer's instructions. Results are shown in Table 13; specific modifications of the siRNAs are indicated in the table, which are the modifications as described herein in Example 5.

TABLE 13 Percent Reduction of PD-L1 Gene with select siRNAs SEQ % Reduction of PD- % Reduction of PD- CC50 ID NO: L1 gene at 50 nM L1 gene at 1 nM (nM) 19-mers (modification pattern as described above in Example 5) 137 D C X 138 D D X 105 D D X 106 C A X 125 B C X 128 C D X 129 D C X 130 D D X 135 C C X 136 D D X 139 D C X 152 C C X 158 D D X 159 D D X 104 C C X 107 C C X 108 D C X 94 C D X 95 C C X 102 D D X 103 B B X 133 A B X 134 A C X 140 B C X 141 C C X 147 C C X 148 D C X 149 C D X 153 C D X 156 D D X 157 D D X 160 D D X 165 D D X 167 D D X 109 D D X 119 D D X 120 D D X 121 D D X 126 B C X 127 B D X 19-mers (modification pattern as described above in Example 5) 283 D D X 284 D D X 285 C D X 286 C D X 287 D D X 288 C D X 289 D D X 290 D D X 291 C D X 292 C D X 293 D D X 294 D D X 295 D D X 296 D D X 297 C D X 298 C D X 299 C D X 300 B D X 301 B D X 302 D D X 303 B D X 304 D D X 305 B D X 306 D D X 307 B D X 308 D D X 309 B D X 310 C D X 311 D D X 312 B C X 313 C D X 314 B C X 315 C C X 317 C D X 318 B D X 319 C D X 320 B C X 321 B D X 322 B D X 323 C D X 324 B C X 325 C D X 326 D D X 327 C D X 328 C D X 329 C D X 330 D D X 331 B C X 332 C D X 333 C D X 334 D D X 335 C D X 336 B C X 337 B C X 338 D D X 339 B C X 340 C D X 341 D D X 342 B D X 343 B D X 344 D D X 345 D D X 346 C D X 347 D D X 348 C D X 349 D D X 350 C D X 351 D D X 352 B D X 354 D D X 373 B C X 374 C C X 375 C C X 376 C D X 377 C C X 378 C C X 379 D D X 380 C D X 21-mers (modification pattern as described above in Example 5) 230 B C X 237 A B X 252 D D X 253 D D X 254 D D X 255 D D X 256 D D X 257 D D X 258 D C X 259 D D X 260 D D X 261 D D X 262 B D X 263 A C X 264 B D X 270 B D X 271 B C X 272 C D X 275 C B X 276 C D X 277 D D X 278 D D X 282 B D X 238 B D X 239 C D X 240 D D X 241 D D X 242 D D X 243 C D X 246 C C X 247 C D X 248 D D X A > 75%-100%; B > 50%-75%; C > 25%-50%; D = 0%-25% X > 20 nM; Y ≤ 20 nM

Example 6: In Vivo Treatment of Mice with siRNA

C57BL/6 mice were provided. One subcutaneous dose of 7.5 mg/kg siRNA or vehicle (phosphate buffered saline) was administered in mice (n=4 per group) on day 0. The siRNA included any of SEQ ID NOs: 2-380, including any modification described herein. On day 3, 10 mg/kg low molecular weight polyI:C (LMW PIC, from Invivogen) was dosed by IV to all groups. Mice were sacrificed 5 hours post-LMW PIC dose. Liver was sectioned and placed in RNALater (Qiagen) for RNA extraction. RNA was extracted from liver samples and PD-L1 gene expression was measured by RT-qPCR. P values were determined from a t-test comparing treatment groups to vehicle control. The values are provided in FIG. 2, and in Table 14.

TABLE 14 Relative Gene Expression for select siRNA sequences Relative P value (t-test) SEQ Gene Compared to ID NO: Modification Expression Vehicle Group Vehicle 1.01 106 3′GalNac4 0.61 0.029 on S strand 134 3′GalNac4 0.54 0.027 on S strand 106 5′VP 0.44 0.002 on AS strand 3′GalNac4 on S strand 134 5′VP 0.38 0.002 on AS strand 3′GalNac4 on S strand

The sequences including the modifications for each of the siRNAs as set forth in Table 14 are provided below in Table 15:

TABLE 15 Sequence modifications for sense strand and antisense strand of siRNAs of Table 14 SEQ ID NO: Sequence (5′ to 3′) 106 S strand: fUpsmApsfUfUfUmAfUfUfUfUmGmAmGfUfCfUmGf UmG-GalNAc4 AS strand: mCpsfApsmCfAmGfAmCfUmCfAmAfAmAfUmAfAmAf UmApsmUpsmU 134 S strand: fUpsmGpsmGfUmGmGfUmGfCfCmGmAfCfUmAfCmAm AmG-GalNAc4 AS strand: mCpsfUpsmUfGmUfAmGfUmCfGmGfCmAfCmCfAmCf CmApsmUpsmU 106 S strand: fUpsmApsfUfUfUmAfUfUfUfUmGmAmGfUfCfUmGf UmG-GalNAc4 AS strand: VPmCpsfApsmCfAmGfAmCfUmCfAmAfAmAfUmAfAm AfUmApsmUpsmU 134 S strand: fUpsmGpsmGfUmGmGfUmGfCfCmGmAfCfUmAfCmAm AmG-GalNAc4 AS strand: VPmCpsfUpsmUfGmUfAmGfUmCfGmGfCmAfCmCfAm CfCmApsmUpsmU

The example siRNAs, including the example sequences and example modifications as described in the examples, are intended as exemplary sequences and modifications. However, it is to be understood that the disclosure relates to any siRNA sequence as set forth herein, having any modification or combination of modifications as set forth herein may be implemented in the examples.

In at least some of the previously described embodiments, one or more elements used in an embodiment can interchangeably be used in another embodiment unless such a replacement is not technically feasible. It will be appreciated by those skilled in the art that various other omissions, additions and modifications may be made to the methods and structures described above without departing from the scope of the claimed subject matter. All such modifications and changes are intended to fall within the scope of the subject matter, as defined by the appended claims.

With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity.

It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to embodiments containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description or claims, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.”

In addition, where features or aspects of the disclosure are described in terms of Markush groups, those skilled in the art will recognize that the disclosure is also thereby described in terms of any individual member or subgroup of members of the Markush group.

As will be understood by one skilled in the art, for any and all purposes, such as in terms of providing a written description, all ranges disclosed herein also encompass any and all possible sub-ranges and combinations of sub-ranges thereof. Any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, tenths, etc. As a non-limiting example, each range discussed herein can be readily broken down into a lower third, middle third and upper third, etc. As will also be understood by one skilled in the art all language such as “up to,” “at least,” “greater than,” “less than,” and the like include the number recited and refer to ranges which can be subsequently broken down into sub-ranges as discussed above. Finally, as will be understood by one skilled in the art, a range includes each individual member. Thus, for example, a group having 1-3 articles refers to groups having 1, 2, or 3 articles. Similarly, a group having 1-5 articles refers to groups having 1, 2, 3, 4, or 5 articles, and so forth.

While various aspects and embodiments have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting, with the true scope and spirit being indicated by the following claims.

All references cited herein, including but not limited to published and unpublished applications, patents, and literature references, are incorporated herein by reference in their entirety and are hereby made a part of this specification. To the extent publications and patents or patent applications incorporated by reference contradict the disclosure contained in the specification, the specification is intended to supersede and/or take precedence over any such contradictory material.

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Although the foregoing has been described in some detail by way of illustrations and examples for purposes of clarity and understanding, it will be understood by those of skill in the art that numerous and various modifications can be made without departing from the spirit of the present disclosure. Therefore, it should be clearly understood that the forms disclosed herein are illustrative only and are not intended to limit the scope of the present disclosure, but rather to also cover all modification and alternatives coming with the true scope and spirit of the invention. 

1. A small interfering RNA (siRNA) that targets human CD274 mRNA, comprising a sense strand and an antisense strand, wherein the antisense strand comprises 18 to 21 nucleotides selected from the group consisting of unmodified nucleotides and modified nucleosides, wherein each modified nucleoside contains a modified sugar, contains a modified nucleobase or is abasic, or both contains a modified sugar and contains a modified nucleobase or is abasic; wherein each linkage between the nucleosides is a phosphorothioate, phosphodiester, phosphoramidate, thiophosphoramidate, methylphosphate, methylphosphonate, phosphonoacetate, amide, boranophosphate, or any combination thereof; and wherein the siRNA is at least 85% complementary to a fragment of human CD274 mRNA.
 2. The siRNA of claim 1, wherein the siRNA comprises zero, one, or two mismatches to the fragment of human CD274 mRNA.
 3. The siRNA of claim 2, wherein the mismatches occur at any one or more of positions 1 or 9 through m, wherein m is the total number of nucleotides in the antisense strand.
 4. The siRNA of claim 2, wherein the mismatches do not occur at a seed region of the siRNA.
 5. The siRNA of claim 4, wherein the seed region is at positions 2-8.
 6. The siRNA of claim 1, wherein the siRNA has a sequence as set forth in any one of SEQ ID NOs: 2-380.
 7. The siRNA of claim 1, wherein the siRNA has 18 nucleotides.
 8. The siRNA of claim 1, wherein the siRNA has 19 nucleotides.
 9. The siRNA of claim 1, wherein the siRNA has 20 nucleotides.
 10. The siRNA of claim 1, wherein the siRNA has 21 nucleotides.
 11. The siRNA of claim 1, further comprising a 2-nucleotide overhang.
 12. The siRNA of claim 11, wherein the 2-nucleotide overhang is non-complementary to the CD274 mRNA.
 13. The siRNA of claim 1, wherein the modified sugar is selected from the group consisting of 2′-OMe, 2′-F, 2′-MOE, 2′-araF, 2′-araOH, 2′-OEt, 2′-O-alkyl, LNA, scpBNA, AmNA, cEt, ENA, and GNA.
 14. The siRNA of claim 1, wherein the antisense strand comprises a 5′-phosphate group or a 5′-phosphate mimic.
 15. The siRNA of claim 14, wherein the 5′-phosphate mimic is a 5′-vinylphosponate.
 16. The siRNA of claim 1, further comprising a targeting moiety.
 17. The siRNA of claim 16, wherein the targeting moiety is conjugated to the siRNA at the 5′ end, 3′ end, or both.
 18. The siRNA of claim 16, wherein the targeting moiety is a fatty acid, GalNAc, folic acid, cholesterol, tocopherol, or palmitate.
 19. The siRNA of claim 1, wherein the modified nucleoside is selected from the group consisting of:

wherein R¹ is hydrogen or C₁₋₇ alkyl.
 20. The siRNA of claim 19, wherein the Base is selected from the group consisting of adenine, guanine, cytosine, 5-methyl cytosine, thymine, and uracil.
 21. A pharmaceutical composition comprising an effective amount of the siRNA according to claim 1 and a pharmaceutically acceptable carrier, diluent, excipient, or combination thereof.
 22. (canceled)
 23. (canceled)
 24. (canceled)
 25. (canceled)
 26. A method for treating hepatitis B in a subject comprising administering to the subject in need thereof an effective amount of an siRNA of claim
 1. 27. A method for treating hepatocellular carcinoma (HCC) in a subject comprising administering to the subject in need thereof an effective amount of an siRNA of claim
 1. 28. The method of claim 27, further comprising administering surgery, radiation therapy, chemotherapy, targeted therapy, immunotherapy, hormonal therapy, or antiviral therapy. 